BENZOIN TINCTURE, COMPOUND

Benzoin Tincture, Compound, USP is an over-the-counter topical medication intended for external use only, containing 1000 mg of benzoin resin per milliliter as the active ingredient and 77 percent alcohol as an inactive ingredient. It is supplied in 16-ounce bottles, equivalent to one pint or 473 milliliters, and is classified as flammable, requiring storage at controlled room temperature between 20°C and 25°C (68°F to 77°F) and strict avoidance of sparks, heat, or flame. The product has a non-extendable shelf life of 36 months, with a mandatory minimum of 31 months of remaining shelf life at the time of receipt by the first government activity. As a regulated medical item, it is subject to FDA oversight and must be labeled and packaged in accordance with Medical Marking Standard No. 1, superseding MIL-STD-129. Each shipment must be accompanied by a current Material Safety Data Sheet, which must also be electronically submitted to DLA.MSDS@DLA.MIL along with the required cover sheet. Packaging must comply with hazardous materials transportation regulations including 49 CFR and ICAO technical instructions. The item is identified by NSN 6505-01-654-9628 and is part of a federal procurement under solicitation SPE2DP-26-T-4129 with a three-bottle quantity, a 20-day delivery requirement, and technical and quality requirements governed by the DLA Master List of Technical and Quality Requirements.