Medi-first Triple Antibiotic Ointment
Product Images NDC 47682-982

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Medi-first Triple Antibiotic (NDC 47682-982). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unifirst First Aid Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Medi-first Plus (Medi First Plustribiotic93473 Nantong Ultrad 1 12 23 (002) Label)

Medi-first Plus (Medi First Plustribiotic93473 Nantong Ultrad 1 12 23 (002) Label)
The packaging label for Medi-First Plus Triple Antibiotic Ointment features the brand name prominently with the active ingredients Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, and Polymyxin B Sulfate 5000 units per gram. It is a topical first aid antibiotic ointment presented in a 0.5 g (1/57 oz) unit with item number 93473, manufactured for Medique Products by Unifirst First Aid Corporation. Label includes drug facts, warnings, directions, storage instructions, and contact information.*
FDA Label Image

Medi-first Tri (Medi First Tribiotic22373 Nantong Ultrad 1 12 23 Label)

Medi-first Tri (Medi First Tribiotic22373 Nantong Ultrad 1 12 23 Label)
Medi-First Plus Triple Antibiotic Ointment box label featuring Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, and Polymyxin B Sulfate 5000 units per gram. The label highlights its use as a first aid antibiotic in 0.5 g packets, with 25 packets per box, manufactured for Medique Products by Unifirst First Aid Corporation.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.