Label: CLEAN CARE HAND SANITIZER- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 74200-0012-1, 74200-0012-2 - Packager: URBANBCL CO LTD
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 19, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
PURPOSE
The convenient Sense Fresh Advanced Instant Hand Sanitizer with Aloe is an antimicrobial liquid that contains 70 percent ethyl alcohol to help reduce the number of germs on hands, and three moisturizers to help keep skin hydrated. No rinsing with water or drying with towels is needed. Alcohol-based hand sanitizers can quickly reduce the number of germs on hands within 30 seconds. The hand sanitizer meets U.S. Food and Drug Administration (FDA) healthcare personnel hand-washing requirements. It’s perfect for on-the-go uses when traveling outside of the home, and fits neatly in purses, backpacks or briefcases.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CLEAN CARE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74200-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) CARBOMER 940 (UNII: 4Q93RCW27E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74200-0012-1 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 2 NDC:74200-0012-2 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/01/2020 Labeler - URBANBCL CO LTD (694794065) Registrant - URBANBCL CO LTD (694794065) Establishment Name Address ID/FEI Business Operations URBANBCL CO LTD 694794065 manufacture(74200-0012)