Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 72264-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biolab International Incorporated for the product Hand Sanitizer (NDC 72264-008). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Uses hand sanitizer to help reduce bacteria on the skin . For occassional and personal domestic use
Warnings
Warnings
for external use only: hands
Flammable. Keep away from fire or flame
Otc - When Using
when using this product, avoid contact with eyes, in case of contact, rinse eyes thoroughly with water, avoid contact with broken skin .
Otc - Stop Use
Stop use and consult a doctor if . irritation or redness develops. condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. children under 6, use only under adult supervision, Not recommended for infants.
For external use only. Do not drink.
If swallowed, seek professional assistance or contact a poison control center.
Dosage & Administration
Directions. Place enough product in your palm to thoroughly spread on both hands and rub into skin until dry.
Storage And Handling
Other information. do not store above 105°F， may discolor some fabics. harmful to wood finished and plastics
Inactive Ingredient
Inactive ingredients acrylates/C10-C30 alkyl acrylate crosspolymer,aloe barbadensis leaf juice, glycerin, maltodextrin, propylene glycol, water , triethanolamine,Fragrance. FD&C Blue No.1, FD&C Yellow No.5
Package Label.Principal Display Panel
Image Of Bottle Label (8oza)
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