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Drug Facts
Antibacterial Hand Sanitizer
FDA Label NDC 73563-080
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Body One Products , Inc. for the product Antibacterial Hand Sanitizer (NDC 73563-080). 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 other, active ingredient, purpose, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 62%
Purpose
Antiseptic
Uses
- for handwashing to decrease bacteria on the skin
- recommended for repeated use.
Warnings
For external use only. Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in the eyes. In case of contact, rinse eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and presist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact poison control center right away.
Directions
- wet hands thoroughly with product
- briskly rub hands together until dry
- supervise children in the use of this product
Other Information
- store at 20° to 20°C (68 to 77° F)
- may discolor certain fabrics
Inactive Ingredients
Water, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,PEG 60 Almond Glycerides, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate,Triisopropanolamine, Fragrance
Principal Display Panel - 1064 Ml Bottle Label
BodyOne
Products
ANTIBACTERIAL
HAND SANITIZER
kills 99.99%
of all germs
(32 FL.OZ. 1064ML)
Principal Display Panel (1064 ML Bottle Label)
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