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 UNILEVER ASIA PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol (75% v/v)

PURPOSE

ANTISEPTIC

USE

Help decrease bacteria on the hands. For use when soap and water are not available.

WARNINGS

For external use only.

Flammable. Keep away from fire or flame. Do not store in car.

Avoid contact with eyes, in case of contact, rinse eyes thoroughly with water immediately.

If irritation develops, discontinue use and consult a doctor.

Keep out of reach of children.

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

DO NOT USE

Do not use:

• On children less than 2 months of age.
• On open skin wounds.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a poison control center right away.

DIRECTIONS

• Wet hands thoroughly with product and rub lightly until dry. Do not wipe off or rinse.

OTHER INFORMATION

• May discolor fabrics or surfaces. Store below 95°F (35°C).

INACTIVE INGREDIENTS

Carbomer, Denatonium Benzoate, Purified Water USP, Tert-butyl Alcohol, Triethanolamine.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUAVE HAND SANITIZER PROFESSIONAL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50069-109
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
WATER (UNII: 059QF0KO0R)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50069-109-11	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020
2	NDC: 50069-109-12	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020
3	NDC: 50069-109-13	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/25/2020

Labeler - UNILEVER ASIA PRIVATE LIMITED (894632699)