Active Ingredient
BENZALKONIUM CHLORIDE 0.1%
Foaming Hand Sanitizer
FDA Label NDC 72036-240
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 Foaming Hand Sanitizer (NDC 72036-240). 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, uses, warnings, when using this product, stop using 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
Antimicrobial
Uses
To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
For external use only.
When Using This Product
avoid contact with eyes. If contact occurs, rinse with water.
Stop Using And Ask A Doctor
if irritation or rash 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
Pump enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.
Inactive Ingredients
Water, Polysorbate 20, Ethylhexyl Methoxycinnamate, Ethylhexyl Sallicylate, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance, Tetrasodium EDTA, DMDM Hydantoin, Sodium Hydroxide, Blue 1, Yellow 5
Package Front And Back Labels
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Front And Back Labels (Ht)
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