SUAVE HAND SANITIZER- alcohol gel

Land: Vereinigte Staaten

Sprache: Englisch

Quelle: NLM (National Library of Medicine)

Wirkstoff:

Alcohol 75%

Verfügbar ab:

UNILEVER ASIA PRIVATE LIMITED

Verabreichungsweg:

TOPICAL

Verschreibungstyp:

OTC DRUG

Anwendungsgebiete:

Antiseptic help decrease bacteria on the hands

Berechtigungsstatus:

OTC monograph not final

Fachinformation

SUAVE HAND SANITIZER- ALCOHOL GEL
UNILEVER ASIA PRIVATE LIMITED
_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._
----------
UNILEVER - SUAVE HAND SANITIZER (75% ETHYL ALCOHOL), 50069-105,
DELIST AS OF 12/31/2022
ACTIVE INGREDIENTS
Alcohol 75%
PURPOSE
Antiseptic
USES
help decrease bacteria on the hands
WARNINGS
For exteral use only
Flammable. Keep away from fire or flame.
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 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℃
INACTIVE INGREDIENTS
Water (Aqua), Carbomer
Triethanolamine.
SUAVE HAND SANITIZER
alcohol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:50069-105
ROUTE OF ADMINISTRATION
TOPICAL
UNILEVER ASIA PRIVATE LIMITED
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 HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:50069-
105-06
236 mL in 1 BOTTLE; Type 0: Not a Combination
Product
05/06/2020
12/31/2022
2
NDC:50069-
105-16
500 mL in 1 BOTTLE; Type 0: Not a Combination
Product
06/17/2020
12/31/2022
3
NDC:50069-
105-11
1000 mL in 1 BOTTLE; Type 0: Not a Combination
Product
06/17/2020
12/31/2022
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICAT