BARBIE HAND SANITIZER- benzalkonium chloride liquid

Barbie Hand Sanitizer by

Drug Labeling and Warnings

Barbie Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ashtel Studios, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

INDICATIONS & USAGE

Use To help reduce bacteria and germs on the skin.

WARNINGS

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.

DOSAGE & ADMINISTRATION

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.

STORAGE AND HANDLING

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

INACTIVE INGREDIENT

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

SPL UNCLASSIFIED SECTION

Smart Care®

barbie.com

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

SMARTCAREUS.COM

Packaging

INGREDIENTS AND APPEARANCE

BARBIE HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70108-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70108-024-01	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/01/2019

Labeler - Ashtel Studios, Inc. (148689180)