Active Ingredient(S)
Alcohol 62-70%(v/v)
Hand Sanitizer
FDA Label NDC 76635-003
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 Hand Sanitizer (NDC 76635-003). 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, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Daily hand sanitizer, to help reduce bacteria on the skin.
Warnings
Flammable.Keep away fire or flame.
For external use only.When using this product do not use in or near the eyes.In case of contact,rinse eyes thotoughly with water.Stop use and ask a doctor of irriration or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.If swallowed,get medical help or contact a poison control center right away.
Directions
Do not shake before use.Squeeze gel onto your palm and massage your hands together until dry.
Other Information
Validity:24 months
Production date:See the package in the bottom.
Inactive Ingredients
Water，Glycerin，Carbomer，Isopropyl Palmitate，Trolamine
Package Label - Principal Display Panel
Label 50ml (Label 50ml)
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