U Instant Hand Sanitizer Classic
FDA Label NDC 73003-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biotek India for the product U Instant Hand Sanitizer Classic (NDC 73003-005). 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 drug facts, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70% v/v
Purpose
Antimicrobial
Uses
Hand Sanitizer to help reduce bacteria on skin.
Warnings
Flammable. Keep away from fire or flame.
For external use only.
When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
• Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using this product.
Other Information:
• Store below 106° F. (41°C)
• May discolor certain fabrics or surfaces
Inactive Ingredients:
Water(Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin,Propylene Glycol, Tocopheryl Acetate, Triethanolamine.
Packaging
Image (7300300501)
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