Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 77664-922
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Beauty Elite Group for the product Hand Sanitizer (NDC 77664-922). 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 - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Hand Sanitizer to help reduce bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from fire or flame
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
Stop use and ask a doctor if irritation 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
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store below 110F (43C)
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Glycerin, Water
Package Label - Principal Display Panel
236 mL NDC: 77664-922-01
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