BENZOIN TINCTURE, COMPOUND

BENZOIN TINCTURE, COMPOUND, USP is an over-the-counter topical medication containing 1000 mg of benzoin resin per milliliter as the active ingredient and 77 percent alcohol as an inactive ingredient, intended for external use only. It is packaged in 16-ounce bottles (473 ml) and classified as a flammable hazardous material requiring strict handling, storage, and shipping protocols to prevent exposure to sparks, heat, or open flame. The product must be stored at controlled room temperature between 20°C and 25°C (68°F to 77°F) and carries a non-extendable shelf life of 36 months, with a mandatory minimum of 31 months of remaining shelf life upon receipt by the first government activity. The item is regulated by the FDA and is subject to comprehensive technical, quality, and packaging requirements, including compliance with Medical Marking Standard No. 1, which supersedes MIL-STD-129. Each shipment must include a current Material Safety Data Sheet (MSDS) delivered both with the product and submitted electronically to DLA.MSDS@DLA.MIL using the required cover sheet P-75, documenting logistics and NSN information. Packaging must meet applicable hazardous materials regulations, including 49 CFR and ICAO guidelines. The item is identified by NSN 6505-01-654-9628 and is procured under solicitation SPE2DP-26-T-4232 with a three-bottle quantity required for delivery within 20 days ADO to APO 09094-3219. Contracting officials must submit referrals via EBS for product specialist verification, including manufacturer and bidder details. Defense information protection applies, and all technical and quality requirements originate from the DLA Master List of Technical and Quality Requirements, with compliance determined by the revision in effect at the time of solicitation or award.