Active Ingredient
Alcohol Denat. 62%
Hand Sanitizer
FDA Label NDC 74177-028
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by K7 Design Group Inc. for the product Hand Sanitizer (NDC 74177-028). 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, use, warnings, when using this product, stop use and ask a doctor if, 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
Antiseptic
Use
for hand-washing to help decrease bacteria on the skin, only when water is not available
Warnings
For external use only. Flammable, keep away from fire and flames.
When Using This Product
■ do not get into eyes.
■ if contact occurs, rinse eyes throughly with water.
Stop Use And Ask A Doctor If
irritation and redness develops and persists.
Keep Out Of Reach Of Children
if swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Sodium Hydroxide, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Yellow 5, Blue 1
Inner Package Label
Inner Package Label (Aloehndsntzr62alchl50ml)
Blister Package Label
Outer Package Label (Aloehndsntzr62alchl50mlblstrpck)
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