FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM- ethyl alcohol solution

FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM by

Drug Labeling and Warnings

FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc., Guangzhou Gotdya Fine Chemical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70 %

Purpose

Antibacterial

PURPOSE

ANTIBACTERIAL

Uses

• 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 do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

When using this product

• avoid contact with eyes. In case of eye contact, flush with water

Keep out of reach of children.

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DIRECTIONS

• Place enough product on your palm to thoroughly cover your hands
• Rub hands together briskly until dry

Inactive ingredients

Water, Isopropyl Alcohol, Propylene Glycol, PEG-12 Dimethicone Crosspolymer, BIS-PEG-12 Dimethicone.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FRESH HAND FOAMING HAND SANITIZER ALCOHOL FOAM 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70415-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70415-203-11	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/04/2020

Labeler - CWGC LA Inc. (034967904)