Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 77512-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Inkwell Global Marketing Corp. for the product Hand Sanitizer (NDC 77512-002). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antibacterial
Indications & Usage
Uses
Hand sanitizer to reduce bacteria on the skin.
Warnings
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - When Using
When using this product do not use in or near the eyes.In case of contact, rinse eyes thoroughly with
water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develops and persists.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact the Poison Control Center right away.
Dosage & Administration
Directions
- Place enough product on hand to cover fully
- Rub hands together until dry
- Children under 6 years of age should be supervised when using this product.
Storage And Handling
Other Information
Store below 110 F.
Inactive Ingredient
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Maltodextrin,Glycerin, Propylene Glycol, Acrylates/C1O-30 Alkyl Acrylate crosspolymer, Triethanoamine, Fragrance, Tocopheryl Acetate.
Package Label.Principal Display Panel
Image Of Bottle Label (2oz)
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