Acyclovir
Product Images NDC 12634-697

4 FDA label images from Apotheca Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acyclovir (NDC 12634-697). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotheca 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

Label (697 71)

Label (697 71)
Packaging label for Acyclovir 800 mg tablets by Apotheca Inc. The label shows the product name, strength, and dosage form (30 tablets). It includes the NDC number 12634-697-71, barcodes, directions for use, storage instructions, manufacturer details, and references to a child-resistant container and tamper-evident closure. The label also compares the product to Zovirax and notes prescription-only status.*
FDA Label Image

Formula1 (Formula1)

Formula1 (Formula1)
Chemical structure of acyclovir showing its molecular framework including nitrogen, oxygen atoms, and carbon chains as depicted in the diagram.*
FDA Label Image

Ssmax (Ssmax)

Ssmax (Ssmax)
Acyclovir pharmaceutical vial label by Apotheca Inc. The label identifies the product as acyclovir but does not provide visible strength, dosage form, or additional details. The design is primarily white with black text and includes blocks of pattern or security printing at the left.*
FDA Label Image

Sstrough (Sstrough)

Sstrough (Sstrough)
Acyclovir topical cream in a 5 g aluminum tube with a green and white label. The label includes the proprietary name acyclovir, strength (5%), and directions for use. The tube is sealed with a white plastic screw cap. This product is labeled by Apotheca Inc. with NDC 12634-697.*

* 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.