BARBIE HAND SANITIZER- benzalkonium chloride liquid 
Ashtel Studios, 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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Barbie Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use To help reduce bacteria and germs on the skin.

WARNING Flammable. Keep away from fire or flame. For external use only • Stop use and ask a doctor if irritation or redness develops and persists.

Keep out of reach of children. • In case of accidental digestion, seek professional assistance or contact a Poison Control Center immediately.

Directions • Place enough product in palm to cover hands and rub hands together briskly until dry.

• Children under 6, use only under adult supervision.

• Not recommended for infants.

Other Information • Do not store above 100° F (38° C). • May discolor some fabrics. • Harmful to wood finishes and plastics.

Inactive Ingredients • Aqua (Water), Hydroxyethylcellulose, Phenoxyethanol, Disodium EDTA, Polysorbate 20, Parfum (Fragrance).

Smart Care®

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BARBIE and associated trademarks and trade dress are owned by, and used under license from Mattel.

©2019 Mattel. All Rights Reserved.

QUESTIONS OR COMMENTS?     

1-877-274-8358 Toll Free in USA • 1-909-434-0911 International COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE DISTRIBUTED BY ASHTELSTUDIOS INC. ONTARIO, CALIFORNIA 91761

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Packaging

image description

BARBIE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-024
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70108-024-0153 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/01/2019
Labeler - Ashtel Studios, Inc. (148689180)

Revised: 10/2019
Document Id: e9e14311-ee68-46fa-bb28-a4da78b0b893
Set id: 47241574-c47f-4715-beb9-8863fb62b444
Version: 1
Effective Time: 20191028
 
Ashtel Studios, Inc.