SUAVE HAND SANITIZER PROFESSIONAL- alcohol gel

Suave Hand Sanitizer Professional by

Drug Labeling and Warnings

Suave Hand Sanitizer Professional by is a Otc medication manufactured, distributed, or labeled by Guangdong Essence Daily Chemical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 75% v/v

purpose

antiseptic

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only.

Flammable, Keep away from heat or flame.

Do not use

• Onchildren less than 2 months of age
• On open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry
• Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

Purified Water USP, Acrylates Copolymer, Glycerin, Triethanolamine, Aminomethyl Propanol

SPL UNCLASSIFIED SECTION

other information

• Store between 15-30℃ (59-86 ℉)
• Avoid freezing and excessive heat above 40℃(104℉)

Packaging

INGREDIENTS AND APPEARANCE

SUAVE HAND SANITIZER PROFESSIONAL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73931-017
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)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73931-017-01	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/27/2020

Labeler - Guangdong Essence Daily Chemical Co., Ltd (529796211)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Essence Daily Chemical Co., Ltd		529796211	manufacture(73931-017)