Active Ingredient
Ethyl Alcohol 62%
Harris Teeter
FDA Label NDC 72036-223
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Harris Teeter for the product Harris Teeter (NDC 72036-223). 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, warnings, when using this product, stop using this product and ask doctor if, keep out of reach of children, directions, uses, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Warnings
Flammable, keep away from fire.For external use only.
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.
Directions
Apply a small amount in your palm and rub hands together briskly until dry. Children under 6 should be supervised when using this product..
Uses
Helps reduce bacteria on the skin
Inactive Ingredients
Water (Aqua), Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, Blue 1, Yellow 5
Package Front And Back Labels
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Front And Back Labels (Ht)
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