HUMASTE HAND SANITIZER- ethyl alcohol gel

HUMASTE Hand Sanitizer by

Drug Labeling and Warnings

HUMASTE Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Swanrose, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 73%

Purpose

Antimicrobial

Uses

Hand sanitizer to reduce microorganisms on the skin.
Use this product when soap and water are not available.

Warnings

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. FLAMMABLE. This product contains ethyl alcohol.Keep away from sources of ignition. Discontinue use if irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. 

KEEP OUT OF REACH OF CHILDREN. 

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

Directions

Read the entire label before using this product.
Place enough product on your palm to thoroughly cover your hands.
Rub hands together briskly until dry.

Inactive Ingredients

Deinoized water, Glycerol Oil, Carbopol, Triethanolamine

SPL UNCLASSIFIED SECTION

73% Alcohol | Self Drying Gel
Rub well until dry

Distributed & Marketed by Swanrose Inc.
SWANROSE, INC.
751 N. SPAULDING AVENUE
LOS ANGELES, CA 90046
PHONE: +1 (310) 266-5812
Made in China

Packaging

INGREDIENTS AND APPEARANCE

HUMASTE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78287-170
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78287-170-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
2	NDC: 78287-170-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
3	NDC: 78287-170-03	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
4	NDC: 78287-170-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
5	NDC: 78287-170-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
6	NDC: 78287-170-06	260 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
7	NDC: 78287-170-07	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
8	NDC: 78287-170-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
9	NDC: 78287-170-09	980 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
10	NDC: 78287-170-10	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/24/2020
11	NDC: 78287-170-11	5000 mL in 1 CAN; Type 0: Not a Combination Product	06/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/24/2020

Labeler - Swanrose, Inc. (117523391)