Hand Sanitizer Pure Experience

Hand Sanitizer Pure Experience Liquid by

Drug Labeling and Warnings

Hand Sanitizer Pure Experience Liquid by is a Otc medication manufactured, distributed, or labeled by Absara Cosmetics S.A.P.I DE C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER PURE EXPERIENCE LIQUID- alcohol liquid 
Absara Cosmetics S.A.P.I DE C.V.

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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Hand Sanitizer Pure Experience

DRUG FACTS

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use:

Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame. For external use only.

Do not ingest, if swallowed seek medical help. Avoid contact with eyes.

Keep out of reach of children. Children under 6yrs old to use under adult supervision.

In case of irritation, discontinue use and consult your doctor.

Directions:

Apply the liquid on the hands and rub gently for 20 seconds until the product evaporates.

Other Information:

Store below 106ºF (41 ºC). May discolor certain fabrics or surfaces.

Inactive ingredients

Demineralized water, glycerin, *fragrance, dmdm hydantoin, aloe barbadensis extract.

*May contain this ingredient.

Package Labeling

Product Label

HAND SANITIZER PURE EXPERIENCE LIQUID 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70956-312
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70956-312-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202007/01/2022
2NDC: 70956-312-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202007/01/2022
3NDC: 70956-312-083780 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/202007/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/01/202007/01/2022
Labeler - Absara Cosmetics S.A.P.I DE C.V. (816161236)
Establishment
NameAddressID/FEIBusiness Operations
Absara Cosmetics S.A.P.I DE C.V.816161236manufacture(70956-312)

Revised: 9/2022
Document Id: 3db39d6a-e4b0-4e4c-8b3f-aceb28346099
Set id: 436ebef7-ac10-4a46-91e4-b4ffbe4f0272
Version: 2
Effective Time: 20220915