Acyclovir Suspension
Product Images NDC 17856-2170

View Photos of 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 Suspension (NDC 17856-2170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

1 (17856 2170 01 Rev. 1 Case Label)

1 (17856 2170 01 Rev. 1 Case Label)
Acyclovir oral suspension, USP 200 mg/5 mL, label showing dosage form as oral suspension and strength. The label includes directions to deliver 5 mL per dose and instructions to shake well before use. It lists preservatives methylparaben 0.1% and propylparaben 0.02%, storage instructions at 15° to 25°C (59° to 77°F), and a warning to keep out of reach of children. The product is distributed by Atlantic Biologicals Corp and packaged by Unit Dose Solutions.*
FDA Label Image

2 (17856 2170 02 Rev. 1 Case Label)

2 (17856 2170 02 Rev. 1 Case Label)
Acyclovir oral suspension label showing a strength of 400 mg per 10 mL, supplied by Atlantic Biologicals Corp. The label includes preservative information, storage instructions, and a quantity of 72 cups. It features the product NDC 17856-2170-02 and has instructions to refer to the package insert for indications and dosage scheduling.*
FDA Label Image

Acyclo-os-structure.jpg (Acyclo Os Structure)

Acyclo-os-structure.jpg (Acyclo Os Structure)
Chemical structure of Acyclovir, showing its molecular configuration with functional groups including amine, carbonyl, and hydroxyl.*

* 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.