Label: ALASKA BEAUTY FRESH HAND ANTISEPTIC CLEANSER- ethyl alcohol gel
- NDC Code(s): 71447-130-00, 71447-130-01
- Packager: LABORATOIRES DRUIDE INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 January 1, 2021
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- DRUG FACTS
- ACTIVE INGREDIENT
- PURPOSE
- USES
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WARNINGS
For external use only. Flammable. Keep away from heat or flame
Do not use
■ in children less than 2 months of age
■ on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS?
- ALASKA BEAUTY HAND ANTISEPTIC CLEANSER 130 mL (NDC 71447-130-00)
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INGREDIENTS AND APPEARANCE
ALASKA BEAUTY FRESH HAND ANTISEPTIC CLEANSER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71447-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ALOE VERA LEAF (UNII: ZY81Z83H0X) EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) LAURETH-7 (UNII: Z95S6G8201) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71447-130-01 1 in 1 BOX 03/24/2020 1 NDC:71447-130-00 130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/24/2020 Labeler - LABORATOIRES DRUIDE INC (245815014) Registrant - LABORATOIRES DRUIDE INC (245815014) Establishment Name Address ID/FEI Business Operations LABORATOIRES DRUIDE INC 245815014 manufacture(71447-130)