Vitastem Ointment
Product Images NDC 71262-002

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Vitastem (NDC 71262-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viaderma Distribution, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Box

Label for Vitastem First Aid & Antibiotic topical ointment containing Tetracycline Hydrochloride 3% at 3.38 fluid ounces (100 ml). The product is distributed by ViaDerma Distribution, Inc., Las Vegas, NV. The label includes a warning to keep the drug away from children and instructions to seek medical assistance for accidental ingestion or poison control contact.*

FDA Label Image

Label

The Vitastem First Aid & Antibiotic topical ointment label features a green and orange color scheme and displays a 0.5 fl oz (15 mL) bottle image. The active ingredient is Tetracycline Hydrochloride 3%. The labeler is ViaDerma Distribution, Inc. Included is drug facts information, usage warnings, directions, and a barcode with NDC 71262-002-15.*

FDA Label Image

Label2

Packaging label for Vitastem First Aid & Antibiotic Topical Ointment by ViaDerma Distribution, containing Tetracycline Hydrochloride 3% as the active ingredient. The label shows a white pump bottle with product name and details, including a 2.0 FL OZ (60 ml) size. The label also includes Drug Facts, usage warnings, directions, inactive ingredients, and distribution information.*

FDA Label Image

Label3

Vitastem First Aid & Antibiotic Topical Ointment by ViaDerma Distribution, containing Tetracycline Hydrochloride 3% as the active ingredient. The 3.38 FL OZ (100ml) bottle is shown with a spray top. The label includes drug facts, directions for use, warnings, inactive ingredients, and manufacturer information including NDC 71262-002-15.*

* 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.