Active Ingredient(S)
Ethyl alcohol 70% Purpose: Antiseptic
Breathe Hand Sanitizer Gel
FDA Label NDC 22431-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blue Cross Laboratories, Inc. for the product Breathe Hand Sanitizer Gel (NDC 22431-010). 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
Use
- to decrease bacteria on the skin that could cause disease.
- recommended for repeated use
Warnings
For external use only- hands
Flammable. Keep away from heat or flame
Otc - When Using
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin. do not inhale or ingest.
Otc - Stop Use
Stop use and ask a doctor if irritation 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 right away.
Directions
- wet hands thoroughly with product and allow to dry without wiping.
- for children under 6 use only under supervision
- not recommended for infants
Other Information
- do not store above 105 F
- may discolor some fabrics
- harmful to wood finishes and plastics
Inactive Ingredients
water, glycerin, fragrance, carbopol, triethanolamine
Package Label - Principal Display Panel
breathe Hand Sanitizer Gel
8 FL OZ (236 mL)
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