DISNEY FROZEN II HAND SANITIZER- alcohol solution 
Best Brand Consumers Products, 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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74530-021

Drug Fact

Active Ingredient(s)

Isopropyl Alcohol 68%. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

To decrease the bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

For external use only.

Flammable. Keep away from heat and flame

Discontinue if skin becomes irritated and ask a doctor

Keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not inhale or ingest

Avoid contact with broken skin

Keep out of reach of children. In case of accidental ingestion, seek professional assitance or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with products and rub untill dry withour wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other information

Do not store above 105F

May discolor some fabrics

Harmful to wooden finishes and plastics

Inactive ingredients

Water, glycerin, propylene glycol, carbomer, sodium hydroxide

Package Label - Principal Display Panel

image description

DISNEY FROZEN II HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74530-021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74530-021-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product05/29/2020
2NDC:74530-021-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product05/29/2020
3NDC:74530-021-03237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/29/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/29/2020
Labeler - Best Brand Consumers Products, Inc. (058304494)
Establishment
NameAddressID/FEIBusiness Operations
Huizhou Bliss Commodity Co., Ltd417467331manufacture(74530-021)

Revised: 1/2022
Document Id: d4a2010c-6c37-75fa-e053-2995a90a7af2
Set id: 04c74240-d016-4321-bd04-0cb27eafbbdf
Version: 2
Effective Time: 20220102
 
Best Brand Consumers Products, Inc.