INSTANT HAND SANITIZER- alcohol spray

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by COSBE LABORATORY INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

ETHYL ALCOHOL 70-75%VN.

Purpose

ANTIMICROBIAL

Use

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN.

Warnings

HIGHLY FLAMMABLE KEEP AWAY FROM FIRE OR FLAME.FOR EXTERNAL USE ONLY, KEEP OUT OF THE REACH

OF CHILDREN. IN CASE OF EYE CONTACT, FLUSH WITH WATER. AVOID CONTACT WITH EYES. IN CASE OF CONTACT

WITH EYES OR MOUTH, RINSE WITH PLENTY OF WATER AND SEEK MEDICAL ADVICE. FOR CHILDREN,USE UNDER ADULT SUPERVISION.

DO NOT USE

WHEN USING

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

INSTANT HAND SANITIZER GEL KILLS 99.99% OF GERMS.USE WHEREVER AND WHENEVER WITHOUT WATER.PUMP

PRODUCT IN PALM OF HAND AND RUB THOROUGHLY UNTIL HANDS ARE DRY.

Other information

STORE BEL0W 110°F( 43°C).

MAY DISCOLOUR CERTAIN FABRIC OR SURFACES.

Inactive ingredients

ALCOHOL, AQUA, GLYCERIN, BUTYLENE GLYCOL, ALOE BARBADENSIS EXTRACT, ARTEMISIA ARGYI LEAF

EXTRACT CNIDIUM MONNIERI EXTRACT, SARGASSUM FUSIFORME EXTRACT, CARBOMER,TRIETHANOLAMINE, FRAGRANCE.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74620-002
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
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SARGASSUM FUSIFORME (UNII: X436TJ4A11)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74620-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2020

Labeler - COSBE LABORATORY INC. (543033650)

Registrant - COSBE LABORATORY INC. (543033650)

Establishment
Name	Address	ID/FEI	Business Operations
COSBE LABORATORY INC.		543033650	manufacture(74620-002)