WATSON HAND SANITIZER- alcohol gel

Watson Hand Sanitizer by

Drug Labeling and Warnings

Watson Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Tash Market Place. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 62%

Purpose

Antimicrobial

Use

• Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product

rinse eyes thoroughly with water.

Stop use and ask a Doctor

if irritation and redness develop condition persists for more than 72 hours.

Keep out of reach of children.

Poison Control Center right away.

Directions

• Rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.

Other information

• May discolor certain fabrics or surfaces

Inactive ingredients

Water, Carbomer, Glycerin, Aminomethyl Propanol, Propylene Glycol, Tocopheryl Acetate, Barbadensis Leaf Extract, Fragrance (Parfun), Blue 1.

Package Labeling:59ml

Package Labeling:237ml

Package Labeling:500ml

Package Labeling:999ml

INGREDIENTS AND APPEARANCE

WATSON HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90061-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90061-011-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2020
2	NDC: 90061-011-02	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2020
3	NDC: 90061-011-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2020
4	NDC: 90061-011-04	999 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/18/2020

Labeler - Tash Market Place (041805793)