Active Ingredient(S)
Benzalkonium Chloride 0.14%
Wet Wipes
FDA Label NDC 76635-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Glamcos Biotech Co.,ltd for the product Wet Wipes (NDC 76635-007). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
For handwashing to decrease bacteria on the skin.
Warnings
For external use only. Keep out of eyes.
In case of eye contact, rinse eyes with water.
Stop use and ask a doctor if redness or irritation develops.
Keep out of sunlight.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Peel back flap on front to pull out a towelette. Reseal the flap. No need ro rinse.
Inactive Ingredients
Alcohol………………….20% Polyaminopropyl Biguanide………………0.1%
Water…………………78.25% Phenoxyethanol…………………………...0.1%
Glycerin…………….. 0.8% Iodopropynyl Butylcarbamate……………0.007%
Propylene Glycol…….0.3% Green Tea Extract…………………………0.3%.
Package Label - Principal Display Panel
Label-400 (Label 400)
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