Acyclovir Ointment
Product Images NDC 72578-082

3 FDA label images from Viona Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acyclovir (NDC 72578-082). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona Pharmaceuticals 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.

Product Images & Figures Index

FDA Label Image

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 01)

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 01)
Chemical structure of acyclovir, showing its molecular arrangement with distinct functional groups including amine and ether substituents.*
FDA Label Image

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 02)

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 02)
Acyclovir Ointment USP 5% label for topical use, containing 15 g of ointment. The label shows the product name, strength, dosage form, and usage route. It includes instructions for use, storage conditions, manufacturer and distributor information. The label features the Viona Pharmaceuticals Inc logo and NDC 72578-082-01.*
FDA Label Image

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 03)

Acyclovir Ointment Usp, 5% (Fcae1dbe A2d4 4a22 A273 6c7e0bca3888 03)
Label for Acyclovir Ointment, USP 5% strength, topical ointment. The packaging indicates a 15 g tube, for prescription use only. Manufactured by Cadila Healthcare Ltd, India, and distributed by Viona Pharmaceuticals Inc, Cranford, NJ. Directions for use and dosage information are provided, along with storage instructions and barcode.*

* 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.