APPLICATOR, SILVER NITRATE

The applicator is a topical medical device containing a fused mixture of 75% silver nitrate and 25% potassium nitrate, designed for targeted clinical use and regulated by the FDA as a prescription-only product. Each applicator measures six inches in length and is packaged in containers of 100 units, with storage requirements specifying a dark, dry, room-temperature environment away from organic or oxidizable materials to maintain stability. The item has a non-extendable shelf life of 24 months and is classified as a Type I (Code M) hazardous material under DLA specifications, necessitating full compliance with applicable hazardous materials regulations including SPE2DP-26-T-4420, 49 CFR, and ICAO guidelines. A current Material Safety Data Sheet (MSDS) must accompany each shipment and be submitted electronically to [email hidden] along with logistics documentation via cover sheet P-75. Procurement is governed by the DLA Master List of Technical and Quality Requirements, with revisions effective as of the solicitation or award date controlling. The NSN is 6505-00-299-9672, the solicitation number is SPE2DP-26-T-4420, and delivery is required within 20 days of award to the specified performance location in WaterVliet, NY. The contracting official must submit a referral through EBS for FDA regulatory confirmation, including manufacturer details, bidder information, and item description.