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LIDOCAINE AND PRILOCAI

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SPE2DP-26-T-4475Federal

Contract Overview

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

AI Contract Overview

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Lidocaine and prilocaine periodontal gel, marketed as ORAQIX at a 2.5%/2.5% concentration, is a microemulsion dental anesthetic supplied in individual blister-packed cartridges, each containing 1.7 grams of gel, with 20 cartridges per carton. Each cartridge comes with a single-use sterile blunt-tipped applicator and must be stored at controlled room temperature between 20°C and 25°C. The product is regulated by the FDA and classified as a prescription-only device with a non-extendable shelf life of 36 months, requiring labeling in compliance with MMS No. 1. Packaging must conform to DLA specifications, including MIL-STD-129 marking, and all technical and quality requirements from the DLA Master List take precedence over commercial standards. The item is identified by NSN 6505-01-656-9640 and manufacturer part number NDC66312-0110-20 from Dentsply Sirona Inc. The contract, issued under solicitation SPE2DP-26-T-4475, requires delivery of three packages to Seymour Johnson Air Force Base in North Carolina within 20 days of order placement, with FOB destination terms and zero tolerance for quantity variance. Shipping must be conducted via traceable means, explicitly prohibiting parcel post. The delivery is scheduled for August 5, 2026, and the contract includes federal acquisition compliance requirements, including referral protocols for FDA-regulated items through EBS and adherence to covered defense information protocols. The purchasing request number is 7017708438, and all packaging and unit of issue must align with DLA’s authorized standards, with point of contact Lawrence Garnett available for coordination.

General Info

Lidocaine/prilocaine gel ORAQIX, 2.5%/2.5%, 20 cartridges per carton, FDA-regulated, FOB destination, delivery to Seymour Johnson AFB by August 5, 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

424210 - Drugs and Druggists' Sundries Merchant WholesalersView NAICS

Place of Performance

BLDG 2803 2803 MEDICAL CAMPUS DR, SEYMOUR JOHNSON AFB, NC, 27531, US

Set-Aside

NONE

Documents

(1)

SPE2DP-26-T-4475.pdf

PDF

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PhaseSolicitation
Posted

Solicitation

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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
Lawrence Garnett
contact@example.gov
+1 (555) 000-0000

Full Description

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LIDOCAINE AND PRILOCAINE,PERIODONTAL GEL
LIDOCAINE AND PRILOCAINE, PERIODONTAL GEL. RX ONLY. UNIT OF ISSUE IS A
PACKAGE CONTAINING 20 CARTRIDGES. ORAQIX (LIDOCAINE AND PRILOCAINE
PERIODONTAL GEL,) 2.5%/2.5% IS A MICROEMULSION. ORAQIX (LIDOCAINE AND
PRILOCAINE PERIODONTAL GEL), 2.5%/2.5%, IS SUPPLIED IN DENTAL CARTRIDGES
THAT PROVIDE 1.7G GEL. INDIVIDUALLY BLISTER-PACKAGED CARTRIDGES OF
ORAQIX ARE DISTRIBUTED IN A CARTON OF 20. EACH INDIVIDUAL BLISTER
PACKAGE ALSO CONTAINS A STERILE BLUNT-TIPPED APPLICATOR. EACH
BLUNT-TIPPED APPLICATOR IS FOR SINGLE USE ONLY. STORE AT 20° TO 25°C
(68° TO 77°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
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
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.
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
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.
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/
DENTSPLY SIRONA INC 0KSX4 P/N NDC66312-0110-20
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
SPE2DP-26-T-4475
SECTION B
PR: 7017708438 PRLI: 0001 CONT’D
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7017708438 0001 PG 3.000
NSN/MATERIAL:6505016569640
DELIVERY (IN DAYS):0020
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. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
PARCEL POST ADDRESS:
HT1004
4TH MDG SGSM PA
CP 919 722 0954
BLDG 2803 2803 MEDICAL CAMPUS DR
SEYMOUR JOHNSON AFB NC 27531
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
HT1004
4TH MDG SGSM PA
CP 919 722 0954
BLDG 2803 2803 MEDICAL CAMPUS DR
SEYMOUR JOHNSON AFB NC 27531
US
M/F: (TCN) HT100462114259
RDD:
PROJ: TP 3
SUPP ADD: 425511 SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 15
DIC: A0A DIST: ADV: 2A FC: J6
Need Ship Date:00/00/0000
SPE2DP-26-T-4475
SECTION B
PR: 7017708438 PRLI: 0001 CONT’D
Original Required Delivery Date:08/05/2026
SPE2DP-26-T-4475 NSN/Part Number: 6505-01-656-9640 Quantity: 3 PG Purchase Request: 7017708438QTY: 3 Delivery: 20 days ADO

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APPLICATOR, SILVER NITR
Solicitation # SPE2DP-26-T-4469
The applicator consists of a 75% silver nitrate and 25% potassium nitrate mixture fused to one end, measuring six inches or 1.524 centimeters, and is intended for topical use only with a prescription requirement. Each unit of issue is a container holding 100 applicators, which must be stored in the original closed package at room temperature in a dark, dry location, away from organic or oxidizable materials. The item is classified as a Type I (Code M) shelf-life item with a non-extendable shelf life of 24 months. It is regulated by the FDA, and buyers must submit a referral in EBS to confirm product details including bidder and manufacturer information. Hazardous materials regulations apply, requiring a current MSDS to be submitted via DLA.MSDS@DLA.MIL and included with each shipment, with packaging compliant to SPE2DP-26-T-4469 and applicable 49 CFR and ICAO standards. Removal of government identification from non-accepted supplies is required, and covered defense information potentially applies. The NSN is 6505-00-299-9672, with a single contract order quantity and a 10-day delivery requirement after award. The solicitation, issued under SPE2DP-26-T-4469, was posted on August 4, 2026, with responses due by August 10, 2026, and is managed by the Department of Defense’s Medical Supply Chain Pharm FSA, with Nicholas Quigley listed as the primary point of contact.
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NAICS: 325412
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HYDROGEN PEROXIDE TOPI
Solicitation # SPE2DP-26-T-4481
Hydrogen Peroxide Topical Solution USP RP001 is a 3% stabilized solution intended for external topical use only, not for ingestion or application to the eyes or large body areas, and must not be used for more than one week. Each unit of issue is a 473-milliliter bottle, requiring tight closure, storage at controlled room temperature, protection from freezing and excessive heat, and must not be shaken. Labeling and packaging must strictly comply with Medical Marking Standard No. 1A dated February 4, 2013, superseding MIL-STD-129, and all packaging must be commercially sealed and designed to prevent damage during transport. The item is regulated by the FDA and classified as a TYPE I (CODE M) item with a non-extendable shelf life of 24 months. As a hazardous material under OSHA’s revised Hazard Communication Standard effective June 1, 2015, suppliers must provide Safety Data Sheets (SDS) and compliant HCS labels per 29 C.F.R. 1910.1200, and must train employees on these requirements. The contract mandates delivery within 20 days to FPO AP 96693, FOB destination, with zero variance in quantity, and prohibits parcel post in favor of traceable shipping methods. The NSN is 6505-00-153-8480, with a contracted quantity of two bottles, procured under solicitation SPE2DP-26-T-4481, and all technical and quality requirements are governed by the DLA Master List, which supersedes ASTM D3951. Approved manufacturers include Medline Industries, LP, Cardinal Health 200, LLC, and McKesson Medical-Surgical Government, with the item identified by multiple NDC and part numbers. All deliveries must be palletized per RP001 requirements and marked per Medical Marking Standard No. 1.
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NAICS: 325411
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CALCIUM CHLORIDE INJEC
Solicitation # SPE2DP-26-T-4471
CALCIUM CHLORIDE INJECTION USP is procured as a 10 mL single-dose plastic syringe containing 1 gram of calcium chloride (100 mg/mL), packaged ten syringes per unit (1 PG = 10 EA), with a mandatory 24-month shelf life from the date of manufacture, no less than 21 months of which must remain at the time of delivery to the government. The product must be labeled in strict accordance with Medical Marking Standard No. 1, including the NSN, manufacturer, CAGE code, date of manufacture, expiration or retest date, contract number, and lot number, and stored at 20 to 25°C (68 to 77°F). The item is regulated by the FDA and requires prior confirmation from the product specialist via EBS referral before award. Packaging must be commercial and designed to protect against damage, with exterior shipping containers ensuring safe, cost-effective transport to the delivery point. All packaging and marking must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and palletization must follow DLA Packaging Requirements for Procurement. The manufacturer is Pfizer Inc, with NDC 00409-1631-10, and the item is identified by NSN 6505-01-655-0700. Delivery is FOB destination in 20 days to Fort Campbell, Kentucky, with zero quantity variance permitted, and shipment must occur via traceable means, excluding parcel post. The contract reference is SPE2DP-26-T-4471, with an original required delivery date of August 5, 2026, and procurement governed by the DLA Master List of Technical and Quality Requirements, which take precedence over all other standards including ASTM D3951.
Medicinal and Botanical Manufacturing

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TOLNAFTATE POWDER, U
Solicitation # SPE2DP-26-T-4483
The contract specifies the procurement of 6 units of TOLNAFTATE POWDER, USP 1%, each unit being 45 grams, for delivery to a U.S. military vessel at FPO AP 96693. The item, identified by NSN 6505-01-480-7897 and NDC 57896-0199-45, must comply with stringent packaging and labeling requirements, including adherence to Medical Marking Standard No. 1, which supersedes MIL-STD-129, and must be commercially packaged in accordance with ASTM D3951 unless specified otherwise by DLA Master List requirements. The product has a non-extendable shelf life of 36 months and must be labeled and marked according to federal medical standards. Delivery is due within 20 days of contract award, with a firm fixed price and zero variance allowed in quantity. Freight must be shipped via the fastest traceable means—parcel post is prohibited—and transportation must follow DLA Procurement Notes C19 and C20. The contract requires FOB destination delivery, with inspection and acceptance occurring at the final destination. All packaging and palletization must conform to DLA Packaging Requirements for Procurement, and the supplier, GERI-CARE PHARMACEUTICALS CORP., must ensure compliance with all technical and quality specifications outlined in the DLA Master List. The solicitation was issued on August 4, 2026, with a response deadline of August 10, 2026, under contract number SPE2DP-26-T-4483.
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DIBUCAINE OINTMENT
Solicitation # SPE2DP-26-T-4472
Dibucaine Ointment USP is a topical pharmaceutical product containing one percent dibucaine as the active ingredient, designed 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 or 59 to 86 degrees Fahrenheit to maintain stability and efficacy. This item has a non-extendable shelf life of 36 months and must be marked in accordance with the latest edition of the Medical Marking Standard No. 1. It is regulated by the FDA and classified as a Type I (Code Q) pharmaceutical item with specific supply chain requirements under DLA standards. The contract, issued under solicitation number SPE2DP-26-T-4472, requires delivery of five packages (PG) to be shipped FOB destination within ten days. The quantity variance is strictly zero percent, meaning exact fulfillment is mandatory. Inspection and acceptance occur at the destination, and packaging must comply with MIL-STD-2073-1E. The NSN is 6505-00-299-9535 and the manufacturer part number is NDC00536-1211-95, supplied by The Harvard Drug Group, L.L.C. All procurement activities are governed by DLA technical and quality requirements referenced in the DLA Master List, and the contracting official must submit an EBS referral to confirm regulatory compliance before award. The point of contact for the solicitation is Alec Deichman, and the place of performance is San Antonio, Texas.
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MOXIFLOXACIN HYDROC
Solicitation # SPE2DP-26-T-4476
Moxifloxacin Hydrochloride Tablets, 400 mg in 30-count bottles, are procured under solicitation SPE2DP-26-T-4476 for delivery to the Navy Expeditionary Central Facility in Williamsburg, VA, with a required delivery window of 20 days. The contract specifies a total quantity of 24 bottles, each containing 30 tablets, with a unit price of $24.00 per bottle and no variance allowed in quantity. The product must comply with stringent packaging and labeling standards as defined by Medical Marking Standard No. 1, superseding MIL-STD-129, and must be shipped in commercial, durable containers that ensure safe transport via common carrier at the lowest cost. Shelf life is strictly limited to 36 months and non-extendable, with storage required at controlled room temperature and protection from high humidity. The item is regulated by the FDA, and bidders must provide full manufacturer details including NDC numbers, with TEVA PHARMACEUTICALS USA, INC. and RISING PHARMA HOLDINGS, INC. identified as potential suppliers. All packaging, marking, and shipment must adhere to DLA’s Master List of Technical and Quality Requirements, and hazardous material provisions apply as per FED-STD-313 and ASTM D3951 where applicable. Shipment must be made by the fastest traceable means, excluding parcel post, and must be palletized per RP001 requirements. The contract mandates delivery FOB destination, with inspection and acceptance occurring upon receipt at the delivery point, and all documentation must reflect compliance with DLA’s unit of issue and procurement standards.
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