Active Ingredient(S)
Alcohol 70%
Hand Sanitizer
FDA Label NDC 76947-199
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jose Lopez for the product Hand Sanitizer (NDC 76947-199). 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, Hand Sanitizer
Use
For hand washing to decrease bacteria on skin
Warnings
For external use only. Flammable. Keep away from fire or flame
Otc - When Using
Stop use and ask a doctor if skin irritation develops
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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.
Inactive Ingredients
glycerin, water, carbomer
Package Label - Principal Display Panel
11000 mL NDC: 76947-199-28
* Please review the disclaimer below.
