Active Ingredient
Ethyl Alcohol %62
Antibacterial Hand Sanitizer
FDA Label NDC 59779-261
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Pharmacy Inc for the product Antibacterial Hand Sanitizer (NDC 59779-261). 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, purpose, directions, warnings, when using this product, stop using this product and ask doctor if, keep out of reach of children, uses, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Directions
Wet hands thoroughly and rub together until dry
Warnings
- For external use only.
- Flammable, keep away from fire or flame.
When Using This Product
Avoid contact with eyes. If contact occurs, rinse with water
Stop Using This Product And Ask Doctor If
irritation or redness develops and lasts
Keep Out Of Reach Of Children
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately
Uses
To help reduce bacteria on the skin
Other Information
Store at a temperature below 110oF (43oC)
Inactive Ingredients
Water (Aqua), Propylene Glycol, Carbomer, Glycerin, Fragrance (Parfum), Isopropyl Myristate, Tocopheryl Acetate, Aminomethyl Propanol, Mannitol, Cellulose, Hydroxypropyl Methylcellulose, Mica, Titanium Dioxide (CI 77891), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Yellow 5 (CI 19140), Yellow 6 (CI 15985).
Questions/Comments?
1-866-428-7327
Package Front And Back Labels
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8oz Front And Back Labels (Eb8)
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