Hand Sanitizer Gel
FDA Label NDC 77188-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Resource One Inc for the product Hand Sanitizer Gel (NDC 77188-002). 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 drug facts, active ingredient:, purpose:, uses:, warnings:, when using this product:, stop and ask a doctor if:, keep out of reach of children:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient:
Ethyl Alcohol 70%
Purpose:
Antiseptic
Uses:
Hand sanitizer to help reduce the bacteria that potentially will cause disease
Warnings:
For External Use Only
Flammable keep away from children
When Using This Product:
Avoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advise.
Stop And Ask A Doctor If:
Irritation and redness develops
Keep Out Of Reach Of Children:
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Wet hands thoroughly with product and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using this product
Inactive Ingredients:
Glycerin, Carbomer
Package Labeling
Label (Label)
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