Aquafire
Product Images NDC 78931-002

View Photos of 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 Aquafire (NDC 78931-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sherlekar Aircare Private Limited, 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

Back Label 5l (Aquafire 5l Liquid Manufacturer Label Back)

Back Label 5l (Aquafire 5l Liquid Manufacturer Label Back)
This is a drug facts label for a hand sanitizer containing 70% ethyl alcohol as an active ingredient. The purpose of this hand sanitizer is to reduce bacteria on hands. The label warns that the product is flammable, should not be used on children less than 2 months of age, and should not be used on open skin wounds. Users are advised to keep the product away from eyes, ears, and mouth, and to rinse thoroughly with water if it comes into contact with eyes, and to seek medical help immediately if swallowed. The product should be placed in the palm of the hand and rubbed until dry. The label also provides information on storage conditions and inactive ingredients. This hand sanitizer is manufactured by Sherlekar Aircare Pvt Ltd, located in Mangalore, India.*
FDA Label Image

Front Label 5l (Aquafire 5l Liquid Manufacturer Label Front)

Front Label 5l (Aquafire 5l Liquid Manufacturer Label Front)
AQUAFIREâ„¢ is a brand of hand sanitizer that comes in liquid form and contains 70% alcohol along with aloe vera. The package size is 5 litres.*

* 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.