Active Ingredient
BENZALKONIUM CHLORIDE 0.1 PERCENT
Foaming Hand Sanitizer
FDA Label NDC 42507-240
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hy-vee Inc for the product Foaming Hand Sanitizer (NDC 42507-240). 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, uses, warnings, when using this product, stop using this product and ask 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
ANTIMICROBIAL
Uses
TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
Warnings
FOR EXTERNAL USE ONLY.
When Using This Product
AVOID CONTACT WITH EYES. IF PRODUCT GETS INTO EYES, RINSE THOROUGHLY WITH WATER.
Stop Using This Product And Ask Doctor If
IRRITATION OR RASH DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
Directions
PUMP DESIRED AMOUNT ONTO HANDS AND RUB UNTIL YOUR SKIN IS DRY. CHILDREN UNDER THE AGE OF 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.
Inactive Ingredients
WATER, POLYSORBATE 20, ETHYLHEXYL METHOXYCINNAMATE, BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, PPG-26-BUTETH-26, PEG-40 HYDROGENATED CASTOR OIL, ALOE BARBADENSIS LEAF JUICE, FRAGRANCE, TETRASODIUM EDTA, DMDM HYDANTOIN, SODIUM HYDROXIDE, BLUE 1 (CI 42090), YELLOW 5 (CI 19140).
Question Or Comments
1-800-289-8343
Front And Back Labels
Image Of Label (Letech)
* Please review the disclaimer below.
