ALASKA BEAUTY ELEMENTS FRESH HAND SANITIZER- ethyl alcohol gel 
LABORATOIRES DRUIDE INC

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.

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ALASKA BEAUTY ELEMENTS FRESH GEL HAND SANITIZER 200 mL

DRUG FACTS

ACTIVE INGREDIENT

Ethyl Alcohol 70%

PURPOSE

Antiseptic

USES

Hand sanitizer to help reduce bacteria that potentially can cause disease.

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.

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away.

DIRECTIONS

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.

■ Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION

■ Store between 15-30C (59-86F)

■ Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS

Water (Aqua), Aloe Barbadensis Leaf Juice*, Glycerin, Eucalyptus Globulus Oil*, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Polyacrylamide, C13-14 Isoparaffin, Laureth-7, FD&C Blue 1.

*Certified organic

QUESTIONS OR COMMENTS?

Call 1-800-263-8888. Outside Canada or U.S dial +1 514 333 8282 or visit www.dermeco.com

ALASKA BEAUTY ELEMENTS FRESH GEL HAND SANITIZER 200 mL (NDC 71447-200-00)

Alaska Beauty Elements Fresh Gel Hand Sanitizer 200 mL

ALASKA BEAUTY ELEMENTS FRESH HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71447-210
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
LAURETH-7 (UNII: Z95S6G8201)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71447-210-011 in 1 BOX04/22/2020
1NDC:71447-210-00200 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/22/2020
Labeler - LABORATOIRES DRUIDE INC (245815014)
Registrant - LABORATOIRES DRUIDE INC (245815014)
Establishment
NameAddressID/FEIBusiness Operations
LABORATOIRES DRUIDE INC245815014manufacture(71447-210)

Revised: 1/2021
Document Id: c77c9bca-ec21-a86d-e053-2a95a90aa0a3
Set id: a400f5a5-d8b4-622c-e053-2a95a90a5742
Version: 2
Effective Time: 20210101
 
LABORATOIRES DRUIDE INC