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TRIAMCINOLONE ACETO

Active
SPE2DP-26-T-4442Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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Triamcinolone acetonide cream USP 0.1% is a prescription-only topical medication supplied in 80-gram tubes, with a total shelf life of 36 months and a requirement that at least 31 months of shelf life remain upon receipt by the first government activity. It must be stored at controlled room temperature between 20–25°C (68–77°F), with allowable excursions between 15–30°C (59–86°F) in accordance with USP standards. The product is subject to stringent FDA regulation and must comply with all DLA Master List of Technical and Quality Requirements, including packaging and labeling standards per Medical Marking Standard No. 1, which replaces MIL-STD-129. Each unit must be commercially packaged in sealed containers to prevent damage, and bulk shipments must be palletized per DLA procurement guidelines. The item is regulated as a Type I (Code Q) drug with a non-extendable 36-month shelf life, and all packaging must be marked in accordance with applicable defense information and hazardous material requirements if applicable. The contract specifies delivery of 16 tubes to Fort Lewis, Washington, with a required delivery date of August 4, 2026, within five days of shipment, using the fastest traceable means excluding parcel post. Supplier information includes NDC codes for Sandoz, Tarro Pharmaceuticals, and AmerisourceBergen, and the unit of issue is a tube (TU). Pricing is fixed at $16.00 per tube with zero variance allowed in quantity.

General Info

16 tubes of triamcinolone acetonide cream, $16 each, deliver to Fort Lewis by August 4, 2026, 31+ months shelf life.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant WholesalersView NAICS

Place of Performance

9141 SANSONE, FORT LEWIS, WA, 98433-9500, US

Set-Aside

NONE

Documents

(1)

SPE2DP-26-T-4442.pdf

PDF

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Timeline

PhaseSolicitation
Posted

Solicitation

Response Deadline

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
Contacts1 person available
OfficeUS
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
View Agency Profile
Office AddressUS
Contacts
DANIEL PORTER
contact@example.gov
+1 (555) 000-0000

Full Description

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TRIAMCINOLONE ACETO
TRIAMCINOLONE ACETONIDE CREAM, USP
RX ONLY; TOPICAL ADMINISTRATION
.
UNIT OF ISSUE IS A TUBE (TU) CONTAINING 80 GRAMS (GM).
.
THE CREAM IS 0.1% TRAIMCINOLONE ACETONIDE (BY WEIGHT).
.
TOTAL SHELF LIFE IS 36 MONTHS.
.
THERE SHALL BE A MINIMUM OF 31 MONTHS OF REMAINING SHELF LIFE
AT THE TIME OF RECEIPT BY THE FIRST GOVERNMENT ACTIVITY.
.
STORE AT CONTROLLED ROOM TEMPERATURE (20-25°C / 68-77°F)
EXCURSIONS PERMITTED FROM 15-30°C (59-86°F)
[SEE USP CONTROLLED ROOM TEMPERATURE]
.
RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS
(IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE
DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB
AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RQ001: TAILORED HIGHER LEVEL CONTRACT QUALITY REQUIREMENTS
(MANUFACTURERS AND NON-MANUFACTURERS)
.
This device or drug is regulated by the FDA. Note to Buyers: The contracting official shall send a referral in EBS to the product specialist for confirmation. Please include bidder name and bidder contact information, manufacturer name, manufacturer part number, and item description. RS020: Shelf-life requirement RS001 for a TYPE I (CODE Q) item with a shelf life of 36 months (non-extendable) applies to this item.
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS
SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED
IN A SUITABLE SEALED UNIT CONTAINER CAPABLE
OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR
BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL
EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN
NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND
SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT
SPE2DP-26-T-4442
SECTION B
THE LOWEST RATE, TO POINT OF DELIVERY CALLED
FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING
STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES
TO MIL-STD-129.
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
SHALL BE MARKED IAW THE LATEST EDITION OF
THE MEDICAL MARKING STANDARD NO. 1.
MMS NO. 1 IS AVAILABLE ONLINE AT:
https://www.dla.mil/Logistics-Operations/Packaging/
AMERISOURCEBERGEN DRUG CORP 1XUY5 P/N NDC00713-0225-80 SANDOZ INC. 0THL4 P/N NDC00168-0004-80 TARO PHARMACEUTICALS U.S.A., INC. 3HFB6 P/N NDC51672-1282-08
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7017701300 0001 TU 16.000
NSN/MATERIAL:6505006041225
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order.
SPE2DP-26-T-4442
SECTION B
PR: 7017701300 PRLI: 0001 CONT’D
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING
REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
RDD 555 SHIPMENT. SHIP BY FASTEST TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
MARKFOR
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
M/F: (TCN) W91M1Z62110040
RDD: 555
PROJ: TP 1
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 02
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:08/04/2026
SPE2DP-26-T-4442 NSN/Part Number: 6505-00-604-1225 Quantity: 16 TU Purchase Request: 7017701300QTY: 16 Delivery: 5 days ADO

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PSYLLIUM HYDROPHILIC M
Solicitation # SPE2DP-26-T-4405
The contract is for the procurement of Psyllium Hydrophilic Mucilloid in 12-gram packets, each containing 25 mg of potassium and 5 mg of sodium, packaged in units of 30 packets per case. This product is regulated by the FDA and must be supplied with its manufacturer’s part number NDC37000-0740-87, sourced from Procter & Gamble Distributing LLC. The item has a non-extendable shelf life of 24 months and must comply with DLA’s technical and quality requirements as defined in the DLA Master List, with packaging and marking strictly governed by Medical Marking Standard No. 1, which supersedes all references to MIL-STD-129. Packaging must meet MIL-STD-2073-1E and DLA-specific packaging requirements, ensuring secure, commercial-grade containment capable of protecting contents during transit. Delivery is FOB destination with no tolerance for quantity variance, and items must be shipped within five days of contract award using the fastest traceable means—parcel post is prohibited. The delivery address is a Navy vessel in FPO AP 96675, with specific shipping and marking instructions governed by DLA’s logistics protocols. The NSN is 6505-01-719-3181, and the contract number is SPE2DP-26-T-4405, with an original required delivery date of August 4, 2026. All bids must include the supplier and manufacturer details for FDA referral through EBS prior to award.
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HYDROGEN PEROXIDE TOPI
Solicitation # SPE2DP-26-T-4396
Hydrogen Peroxide Topical Solution, USP, is a 3% stabilized topical solution intended for external use only, with clear warnings against use in the eyes or over large body areas and a maximum usage duration of one week. Each unit is a 473-milliliter (16-fluid-ounce) bottle, requiring tight closure, storage at controlled room temperature, protection from freezing and excessive heat, and no shaking. Packaging and labeling must comply with Medical Marking Standard No. 1A dated February 4, 2013, superseding MIL-STD-129, and all units must be sealed in commercial containers suitable for transit and protected from damage. The product is regulated by the FDA and classified as a Type I (Code M) item with a non-extendable shelf life of 24 months. Suppliers must provide Safety Data Sheets (SDS) conforming to 29 C.F.R. 1910.1200 and Hazard Communication Standard (HCS) compliant labels as of June 1, 2015, and must train employees on these requirements. All packaging and shipping must meet commercial standards and ensure safe delivery at the lowest cost to the destination. The item is identified by NSN 6505-00-153-8480, with a purchase request number of 7017684184 and a quantity of 20 bottles. Delivery is FOB destination within 20 days, with zero variance allowed. Solicitation number SPE2DP-26-T-4396, posted August 2, 2026, requires response by August 10, 2026. Approved manufacturers include McKesson, Cardinal Health, and Medline Industries. The contract is administered by the Department of Defense’s Medical Supply Chain, with delivery to Pineville, LA, and point of contact Patrell Postell. All requisitions previously associated with DMLIIS Request ID 1721935 under ACC-L have been canceled without replacement, transitioning to ACCY.
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NAICS: 456199
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LUBRICANT, SURGICAL
Solicitation # SPE2DP-26-T-4417
The contract is for surgical lubricant, a sterile, latex-free, water-soluble jelly containing parabens, with each foil packet containing 2.7 grams and packaged in boxes of 144 packets as the unit of issue. The product must comply with strict technical and quality requirements outlined in the DLA Master List, and all packaging and marking must adhere to the Medical Marking Standard No. 1, which supersedes MIL-STD-129. The item has a non-extendable shelf life of 36 months and must be stored at 20°C to 25°C (68°F to 77°F). It is regulated by the FDA and classified as a TYPE I (CODE Q) item with specific shelf-life controls. The supplier, MEDLINE INDUSTRIES, LP, must provide the item under part number MDS032273H, and the NSN is 6505-01-626-5774. The contract requires delivery of one box within 20 days to a designated military destination, with FOB destination terms and zero variance permitted on quantity. All packaging must be commercial-grade, sealed, and designed for safe transit with minimal cost to ensure unharmed delivery. The item must be marked according to MMS No. 1, and transportation details are governed by DLAD procedural notes. The contract is issued under solicitation SPE2DP-26-T-4417 with a required delivery date of August 4, 2026, and the point of contact is Nicholas Quigley of the Department of Defense’s Medical Supply Chain.
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DIBUCAINE OINTMENT
Solicitation # SPE2DP-26-T-4418
Dibucaine Ointment USP is a topical pharmaceutical product containing 1 percent dibucaine as the active ingredient, formulated for rectal administration and external use only. It is supplied in a collapsible tube and includes a rectal applicator, with each unit of issue being a single package containing one ounce or 28 grams of ointment. The product must be stored at temperatures between 15 and 30 degrees Celsius (59 to 86 degrees Fahrenheit) and carries a non-extendable shelf life of 36 months, classified as a TYPE I (CODE Q) item. Packaging and marking must comply with the latest edition of the Medical Marking Standard No. 1 and MIL-STD-2073-1E, ensuring proper government logistics handling. The item is regulated by the FDA, and procurement requires a referral through EBS to verify compliance before award. This product is procured under solicitation SPE2DP-26-T-4418 with a required delivery within five days to Offutt AFB, zip 68113-1044, under FOB destination terms. Quantity is fixed at one package (PG) with zero variance allowed, and inspection and acceptance occur at the delivery point. The National Stock Number is 6505-00-299-9535, and the NDC code is 00536-1211-95. The supplier is The Harvard Drug Group, L.L.C., and the procurement is managed by the Department of Defense’s Medical Supply Chain Pharmacy FSA. Contract data specifies a response deadline of August 10, 2026, with technical and quality requirements governed by the DLA Master List of Technical and Quality Requirements. Covered Defense Information may apply under RD003, and removal of government identification from non-accepted supplies is required per RQ011.
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SUMATRIPTAN SUCCINATE
Solicitation # SPE2DP-26-T-4415
Sumatriptan Succinate Tablets, 100 mg, are supplied in a bottle of nine tablets and are indicated for the acute treatment of migraine with or without aura in adults. The product must be stored at controlled room temperature between 20 to 25°C (68 to 77°F) and protected from light, in compliance with USP standards. The item is regulated by the FDA and subject to strict shelf-life requirements: it has a non-extendable shelf life of 24 months as a Type I CODE M item, and must be marked according to the latest edition of Medical Marking Standard No. 1 and MIL-STD-129 for packaging and labeling. Packaging and palletization must adhere to DLA’s Packaging Requirements for Procurement and MIL-STD-2073-1E, with no tolerance for quantity variance. The contract specifies delivery FOB destination within 20 days, with inspection and acceptance occurring at the destination. The supplier is identified as MYLAN PHARMACEUTICALS INC with NDC 00378-5632-59, and the item is procured under NSN 6505-01-727-8704. Delivery is to a U.S. military address in APO AE 09094-3219, with freight originating from Ramstein, Germany. The solicitation number is SPE2DP-26-T-4415, with a required delivery date of August 4, 2026, and bid responses due by August 10, 2026. Technical and quality requirements are governed by the DLA Master List, and the contracting official must submit a referral through EBS for FDA product validation prior to award.
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PETROLATUM, WHITE
Solicitation # SPE2DP-26-T-4447
The contract specifies the procurement of Petrolatum, White, USP, with a unit of issue of 1 TU equaling 28 mg, and a total quantity of 1 TU required. The item has a non-extendable shelf life of 36 months and must be packaged in accordance with the Medical Marking Standard No. 1, which supersedes MIL-STD-129, and all packaging must ensure protection against damage and compliance with commercial shipping standards for safe delivery to the destination. The material is not classified as hazardous under FED-STD-313 and must be commercially packaged per ASTM D3951, though any conflicting requirements from the DLA Master List of Technical and Quality Requirements take precedence. Labeling and marking of all containers must strictly follow the latest edition of Medical Marking Standard No. 1, and packaging must be palletized per RP001, using the designated unit pack configuration and ensuring the lowest freight cost to the specified delivery point. Delivery is required within five days of award, FOB destination, with zero variance allowed in quantity, and inspection and acceptance occur upon arrival. The item is to be shipped by the fastest traceable means, excluding parcel post, to the government address in Morrisville, NC, with explicit instructions to avoid using outdated or non-compliant marking systems. The solicitation is issued under contract SPE2DP-26-T-4447, with a required delivery date of August 4, 2026, and the item is identified by NSN 6505-00-254-5527 and NDC 53329-0068-01, supplied by Medline Industries, LP.
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OMEPRAZOLE EXTENDED-RE
Solicitation # SPE2DP-26-T-4402
Omeprazole extended-release capsules, 20 mg in 30-count units, are procured under solicitation SPE2DP-26-T-4402 for government use with a total requirement of 23,000 units across multiple contract line items. Each unit must be packaged in sealed containers that protect against damage and shipped in commercial exterior containers to ensure safe, low-cost delivery to designated government destinations. The product must be stored at controlled room temperature between 20 and 25 degrees Celsius and carries a non-extendable shelf life of 18 months. All packaging and labeling must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and conform to DLA packaging requirements including palletization and hazardous material handling per Fed-Std-313 and ASTM D3951 where applicable. The item is regulated by the FDA and requires supplier verification through EBS referral. Shipments must be sent by traceable means only, excluding parcel post, and deliveries are required FOB destination within five days of ship date. The original required delivery date for all orders is no later than August 4, 2026, with one contract line due by July 30, 2026. The contract includes multiple delivery addresses across Fort Lewis, Washington, and Watervliet Arsenal, New York, with strict adherence to unit of issue and quantity per unit pack specifications. The sole source manufacturers listed include Astra Pharmaceutical Products Inc, Sandoz Inc, Amerisource Health Services LLC, and Golden State Medical Supply Inc, with NDC numbers specified for each.
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PERMETHRIN CREAM RINSE
Solicitation # SPE2DP-26-T-4404
Permethrin Cream Rinse is a 1% w/v topical pharmaceutical product packaged in a 2 fluid ounce plastic squeeze bottle, each unit including a comb for application. The product has a 24-month shelf life, with a mandatory minimum of 21 months remaining at the time of receipt by the first government activity. It is regulated by the FDA and subject to strict medical acquisition standards, including commercial packaging requirements that ensure the unit is sealed and protected from damage, and shipments are placed in suitable exterior containers for safe transport at the lowest carrier rate. All items must be marked in compliance with Medical Marking Standard No. 1, replacing all references to MIL-STD-129. The product is hazardous and requires compliance with Federal Standard No. 313-E, mandating submission of current Safety Data Sheets (SDS) formatted per 29 C.F.R. 1910.1200 and appropriate Hazard Communication Standard labels prior to award. Each shipment must include a physical copy of the SDS, and suppliers must submit these documents to DLA.MSDS@DLA.MIL with a completed cover sheet. Packaging must meet 49 CFR and ICAO regulations for hazardous materials. Technical and quality requirements are governed by the DLA Master List, and the procurement is subject to Hazard Communication Standard updates. The NSN is 6505-01-256-4972, and the solicitation requires delivery of five units within five days of award, with the contract issued under SPE2DP-26-T-4404 by the Department of Defense, Medical Supply Chain Pharm FSA.
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ALBUTEROL SULFATE INHA
Solicitation # SPE2DP-26-T-4437
Albuterol Sulfate Inhalation Aerosol with HFA is a prescription-only medication for oral inhalation, with each actuation delivering 108 micrograms of albuterol sulfate equivalent to 90 micrograms of albuterol base, supplied in an 8.5-gram canister containing 200 metered doses. The product must be stored at room temperature between 59°F and 77°F, protected from extreme heat or cold, and must not be punctured, exposed to flames, or stored near heat sources, as temperatures above 120°F may cause the canister to burst. It is subject to a non-extendable 24-month shelf life and must be labeled with the National Stock Number, manufacturer name, date of manufacture, expiration date, contract number, and lot number. All packaging and marking must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and must be shipped in sealed commercial unit containers and approved shipping containers suitable for safe transport at the lowest rate to the delivery point specified. The product is regulated by the FDA and requires submission of Safety Data Sheets and Hazard Communication Standard-compliant labels as mandated by OSHA’s Globally Harmonized System, with supplier training on these requirements. Delivery is FOB destination within five days, with zero tolerance for quantity variance, and inspection and acceptance occur at the delivery point. The contract is issued under solicitation SPE2DP-26-T-4437 for a quantity of 12 units, with the National Stock Number 6505015436562, and references applicable DLA technical and quality requirements contained in the DLA Master List.
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