HAND SANITIZER- alcohol solution

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Huizhou Bliss Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75%

Purpose

Sanitizer

Use

• to decrease bacteria on the skin that could cause disease.
• recommended for repeated use.

KEEP OUT OF REACH OF CHILDREN

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

warnings:

Flamable, keep away from heat and flame

For external use onl-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness or itching occurs.

When using this product

• keep out of eyes, in case of contact with eyes, immediately flush with water and call a doctor.
• avoid contact with broken skin

Stop use and ask a doctor if Irritation and redness develops

Directions

put a thumb size amount in your palm and rub hands together briskly until dry.

Other Information

• do not store in temperatures over 118℉
• children under 6 years of age should be supervised while using this product
• may discolor certain fabrics

Inactive ingredients

Water, glycerin, propyene glycol, carbomer, sodium hydroxide

Packaging

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74274-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74274-008-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/18/2020

Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)

Registrant - Huizhou Bliss Commodity Co., Ltd (417467331)

Establishment
Name	Address	ID/FEI	Business Operations
Huizhou Bliss Commodity Co., Ltd		417467331	manufacture(74274-008)