Drug Facts
ACTIVE INGREDIENT
Ethyl Alcohol 62%
Klar And Danver Instant Hand Santizer
FDA Label NDC 33992-8010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Greenbrier International, Inc. for the product Klar And Danver Instant Hand Santizer (NDC 33992-8010). 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, purpose, use, warnings, when using this product, sop use andask 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
Hand sanitizer to help decrease bacteria on the skin.
When water, soap and towel are not available
Recommended for repeated use
Warnings
For external use only.
Flammable. Keep away from fire and flame
Do not apply around eyes. Do not use in ears and mouth
When Using This Product
avoid contat with eyes. In case of contact flush with water.
Sop Use Andask A Doctor If
redness or irritation develop and persist formore than 72 hours.
Keep Out Of Reach Of Children
Children must be supervised in use of this product
Directions
pump as needed ito your palms and thoroughly spread on both hands
rub into skin until dry.
Other Informatio
Store at 20C (68 to 77F)
may discolor fabrics
Inactive Ingredients
Water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomer, fragrance.
Other
DISTRIBUTED BY GREENBRIER INTERNATIONAL INC
500 VOLVO PARKWAY, CHESAPEAKE, VA 23320. MADE IN MEXICO
Product Labeling
Labels (Label)
Label2 (Label2)
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