Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 79008-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Grupo Delveg, S.a. De C.v. for the product Hand Sanitizer (NDC 79008-001). 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
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help to decrease bacteria on the skin that could cause disease. Recommended for repeted use.
Warnings
For external use only: hands. Flammable. Keep away from fire or flame.
Otc - When Using
Keep out of eyes, in case of contact, flush thoroughly with water. Avoid contact with broken skin. Do not inhale nor ingest.
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 Poisson Control Center immediately.
Directions
- Put enough product in hands to cover them, rub them together briskly until dry.
- Children under 6 years old need adult supervision to use this product.
Other Information
- Store in a cool, dry place at a temperature from 32°F to 95°F.
Inactive Ingredients
carbomer, demineralized water, disodium EDTA, glycerin and triethanolamine.
Package Label - Principal Display Panel
000 mL NDC: 79008-001-00
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