Sanitizer
Product Images NDC 70143-1002

2 FDA label images from Gandang Kalikasan Usa Inc. · 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 Sanitizer (NDC 70143-1002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gandang Kalikasan Usa 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

All-natural Sanitizer Cool Burst 50ml Pdp (All Natural Sanitizer Cool Burst 50ml Pdp)

All-natural Sanitizer Cool Burst 50ml Pdp (All Natural Sanitizer Cool Burst 50ml Pdp)
Label for human nature All-Natural Sanitizer Cool Burst, 1.7 fl. oz. (50 ml). The label highlights claim of killing 99.99% of germs with 100% no harmful chemicals. It is certified by the Natural Products Association. The label includes ingredient information, usage instructions, manufacturer details indicating it is made in the Philippines for Gandang Kalikasan USA Inc., and symbols for cruelty-free and biodegradable packaging.*
FDA Label Image

Cool Burst Drug Facts (Cool Burst Drug Facts)

Cool Burst Drug Facts (Cool Burst Drug Facts)
Label panel of Sanitizer by Gandang Kalikasan USA Inc. showing Drug Facts with active ingredient Ethyl Alcohol 60% as antiseptic, usage directions, warnings about flammability and safety, and inactive ingredients such as aqua (water), Mentha piperita leaf essential oil, Mentha arvensis leaf essential oil, and Aloe barbadensis leaf juice. The label emphasizes all-natural sanitizer, cool burst scent, and claims 99.99% germ kill, with a volume of 1.7 fl oz (50 ml).*

* 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.