FOASU DAILY HAND SANITIZER GEL- alcohol gel

FOASU DAILY HAND SANITIZER gel by

Drug Labeling and Warnings

FOASU DAILY HAND SANITIZER gel by is a Otc medication manufactured, distributed, or labeled by HANSCOS Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70%

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 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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Put nough produt in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product

Other information

• Store below 110°F (43°C)
• May discolor certain fabrics or surfaces

Inactive ingredients

WATER, GLYCERIN, PEG-60 HYDROGENATED CASTOR OIL, CARBOMER, TRIETHANOLAMINE, CAMELLIA SIMENSIS LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, MENTHA PIPERITA (PEPPERMINT) OIL, LIMONENE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOASU DAILY HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77964-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEPPERMINT OIL (UNII: AV092KU4JH)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77964-001-01	30 mL in 1 TUBE; Type 0: Not a Combination Product	05/15/2020
2	NDC: 77964-001-02	50 mL in 1 TUBE; Type 0: Not a Combination Product	05/15/2020
3	NDC: 77964-001-03	100 mL in 1 TUBE; Type 0: Not a Combination Product	05/15/2020
4	NDC: 77964-001-04	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/15/2020
5	NDC: 77964-001-05	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/15/2020

Labeler - HANSCOS Co.,Ltd. (688494423)

Registrant - HANSCOS Co.,Ltd. (688494423)

Establishment
Name	Address	ID/FEI	Business Operations
HANSCOS Co.,Ltd.		688494423	manufacture(77964-001)