Active Ingredient(S)
Benzalkonium Chloride 0.12%. Purpose: Antibacterial
Hand Sanitizer
FDA Label NDC 22431-150
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 for the product Hand Sanitizer (NDC 22431-150). 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, stop use and ask a doctor, 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
Antibacterial, Hand Sanitizer
Use
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only - hands
Otc - When Using
- Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- do not inhale or ingest
Stop Use And Ask A Doctor
if skin irritation develops.
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 adult supervision
- not recommended for infants
Inactive Ingredients
Water, glycerin, propylene glycol, Aloe barbadensis leaf extract, tocopheryl acetate, fragrance, triethanolamine, carbomer
Package Label - Principal Display Panel
89 mL NDC: 22431-150-01
Pdp (22431 150 01)
236 mL NDC: 22431-150-02
Pdp (22431 150 02)
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