JOJO SIWA 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.

----------

Jojo Siwa 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®

©2019 Viacom International Inc. Al Rights Reserved. Nickelodeon and all related titles and logos are trademarks of Viacom International Inc. JoJo Siwa is a trademark of JoJo Siwa Entertainment, LLC.

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 ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

Packaging

image description

JOJO SIWA HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-022
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:70108-022-0153 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: 39e9b2c7-4705-4b82-ab66-a00f2771f755
Set id: 3487b40d-158f-4dae-9160-11bece55448b
Version: 1
Effective Time: 20191028
 
Ashtel Studios, Inc.