Instant Hand Sanitizer Classic Liquid
FDA Label NDC 52000-434
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Instant Hand Sanitizer Classic (NDC 52000-434). 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, otc - keep out of reach of children, directions, inactive ingredients, 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% v/v
Purpose
Antimicrobial
Uses
hand sanitizer to help reduce bacteria on the skin.
Warnings
For external use only.
Flammable. Keep away from heat and flame.
When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.
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.
Inactive Ingredients
aqua (water), acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl propanol, aloe barbadensis leaf juice, denatonium benzoate, fragrance, glycerine, propylene glycol, tocopheryl acetate
Packaging
Instanthandsanitizerclassic (52000434 2)
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