Active Ingredient
Ethyl Alcohol 80%
Hand Sanitizer
FDA Label NDC 52985-903
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anhui Oasis Disinfection Products Co., Ltd for the product Hand Sanitizer (NDC 52985-903). 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, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Hand sanitizer to help reduce bacteria on the hands
To help decrease bacteria on the skin when water, soap and towel are not available
Warnings
Flammable. Keep away from fire or flame. For external use only, not on face
■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 a doctor if imitation or rash appears and lasts
Otc - Keep Out Of Reach Of Children
■Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
1 If signs of rash occur, discontinue use and seek medical advice
■Keep container tightly closed
Directions
■Apply small amount onto your palm, not on open wound
■Rub all parts of hands until dry without rinse
Children under 6 years of age should be supervised during use
Other information
Sore below 86°F (30°C)
1 May discolor certain fabrics or surfaces
■Use within 12 months after open
Inactive Ingredients
boiled cold water, Glycerol, hydrogen peroxide
Package Label.Principal Display Panel
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