HOT WHEELS 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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HOT WHEELS 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).

HOTWHEELS.COM

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

© 2019 Mattel. All Rights Reserved 

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1-877-274-8358 Toll Free in USA + 1-909-434-0911 International COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE 

DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

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Packaging

untitled

HOT WHEELS HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-025
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:70108-025-0153 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: 84f3e709-1b6e-4d67-81a3-3840bce1f4a0
Set id: e5067ce6-96fb-4ee3-acf7-0e1e8567cee0
Version: 1
Effective Time: 20191029
 
Ashtel Studios, Inc