Hand Sanitizer
FDA Label NDC 73752-319
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Specialty Graphics for the product Hand Sanitizer (NDC 73752-319). 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, indications & usage, warnings, keep out of reach of children, dosage & administration, 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 62%
Purpose
Antiseptic
Indications & Usage
Use Decreases bacteria on hands
Warnings
Warnings For external use only
Flammable Keep away from fire or flame
Keep out of eyes In case of eye contact, immediately flush with water and get medical help.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Dosage & Administration
Directions Squeeze onto hands and rub hands together briskly until dry.
Do Not Store Above 110°F
Non-staining, may discolor certain fabrics.
Inactive Ingredients
Deionized Water, Carbomer, Triethanolamine, Aloe Barbadensis Gel, Fragrance Glycerin, Propylene Glycol, Vitamin E.
Packaging
Hndsntr (Specialty)
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