Sanitizer
Product Images NDC 70143-1000

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 70143-1000). 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.

FDA Label Image

All-natural Sanitizer Florall Burst Drug Facts (All Natureal Sanitizer Floral Burst Drug Facts)

All-natural Sanitizer Florall Burst Drug Facts (All Natureal Sanitizer Floral Burst Drug Facts)
Drug Facts panel for Sanitizer with active ingredient Ethyl Alcohol 60% as an antiseptic. It includes uses for decreasing bacteria on skin and recommendations for repeated use, warnings for external use only, flammability, and precautions to keep out of reach of children. Directions instruct to shake well and spray on hands, rubbing thoroughly. Lists inactive ingredients: aqua, fragrance (al-natural), and Aloe Barbadensis leaf juice.*
FDA Label Image

All-natural Sanitizer Floral Burst Pdp (All Natureal Sanitizer Floral Burst Pdp)

All-natural Sanitizer Floral Burst Pdp (All Natureal Sanitizer Floral Burst Pdp)
Label for human nature ALL-NATURAL Sanitizer Floral Burst, 1.7 fl. oz. (50ml) by Gandang Kalikasan USA Inc. The label highlights the product's all-natural ingredients, certification by the Natural Products Association, and claims to kill 99.99% of germs without harmful chemicals. It includes usage instructions, ingredients, manufacturer information, cruelty-free and biodegradable logos, and a floral design.*

* 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.