Triple Antibiotic Plus
Product Images NDC 59450-823

2 FDA label images from The Kroger Co. · 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 Triple Antibiotic Plus (NDC 59450-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Kroger Co., 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

268d8196-figure-01 (268d8196 Figure 01)

268d8196-figure-01 (268d8196 Figure 01)
The packaging label for Kroger Triple Antibiotic Plus Maximum Strength ointment features a blue background with white text. It identifies the product as a maximum strength triple antibiotic ointment plus pain relief, containing Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride. The net weight is 1 oz (28 g). The label states it helps prevent infection in minor cuts, scrapes, and burns plus provides topical pain relief. The Kroger Co. logo is prominently displayed.*
FDA Label Image

268d8196-figure-02 (268d8196 Figure 02)

268d8196-figure-02 (268d8196 Figure 02)
Drug Facts panel for Triple Antibiotic Plus Maximum Strength by The Kroger Co. Lists active ingredients per gram: Bacitracin zinc 500 units, Neomycin sulfate USP 3.5 mg, Polymyxin B sulfate USP 10,000 units, and Pramoxine hydrochloride USP 10 mg. Includes usage instructions, warnings, directions for adults and children 2 years and older, allergy alert, and inactive ingredient white petrolatum. Provides storage information, a consumer helpline number, and advises external use only.*

* 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.