Active Ingredient(S)
Ethyl Alcohol 65% w/w.
Hand Sanitizer
FDA Label NDC 62742-4191
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Allure Labs Inc for the product Hand Sanitizer (NDC 62742-4191). 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 microorganisms on the skin.
- Recommended for repeat use.
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, rise eyes thouroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs 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
- Wet hands thoroughly with product
- Allow to dry without wiping
- Not recommended for infants
- For children under 6, use only under adult supervision
Other Information
- Store at room temperature
- Do not freeze
- May discolor certain fabrics or surfaces
- Do not store above 105 °F
Inactive Ingredients
Water(aqua), Glycerin, Acrylates Copolymer, Sodium Hydroxide, Fragrance (parfum), Benzyl Benzoate, Citral, Geraniol, Hexyl Cinnamaldehyde, linalool
Package Label - Principal Display Panel
Birdzeyelabs.com
Dist. and sold by Birdzeye Labs, LLC
San Mateo, CA USA
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