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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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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:74530-021
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:74530-021-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/29/2020
2	NDC:74530-021-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/29/2020
3	NDC:74530-021-03	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/29/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/29/2020

Labeler - Best Brand Consumers Products, Inc. (058304494)

Name	Address	ID/FEI	Business Operations
Establishment
Huizhou Bliss Commodity Co., Ltd		417467331	manufacture(74530-021)

Revised: 5/2020

Document Id: a6d08de2-de4a-43fa-e053-2995a90a379b

Set id: 04c74240-d016-4321-bd04-0cb27eafbbdf

Version: 1

Effective Time: 20200529

Best Brand Consumers Products, Inc.