Active Ingredient
Ethyl Alcohol 62%
Dawnmist Alcohol Hand Sanitizer Gel
FDA Label NDC 65517-1023
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dukal Llc for the product Dawnmist Alcohol Hand Sanitizer (NDC 65517-1023). 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, warning, 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
To decrease bacteria on the skin that could cause disease
Warning
For external use only
Flammable, keep away from fire or flame.
When Using This Product
Keep out of eyes, ears and mouth. In case of contact with eyes, flush thoroughly with water.
Stop Use And Ask A Doctor If
irritation or redness develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact Poison Control Center right away.
Directions
wet hands thoroughly with products and allow to dry without wiping.
for children under 6, use only under adult supervision
Other Information
Avoid freezing and excessive heat above 104°F
Inactive Ingredients
Acrylates/C10-30Alkyl Acrylate Cross Polymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water
Principle Display Panel
Hs8004 (Hs8004)
DawnMist ®
Hand Sanitizer
Drug Facts
Active Ingredient Purpose
Ethyl alcohol 62%.........Antiseptic
REF HS8004
4 FL. OZ. (118 ml)
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