SINOFRESH FOAMING HAND SANITIZER- foaming hand sanitizer aerosol, foam

SinoFresh Foaming Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

Warnings

Warnings

For External Use Only

When using this product

Do not spray in eyes. If in eyes rinse with water

Stop Use and ask a Doctor

If irritation or rash develops and lasts

INACTIVE INGREDIENT

Inactive Ingredients Water (Aqua), Carbamide

ACTIVE INGREDIENT

Active Ingredients Purpose

Benzalkonium Chloride 0.13%……………….….Antiseptic

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.

PURPOSE

Uses Hand Sanitizer to help reduce bacteria on the skin that could cause disease

Recommended for repeated use

DOSAGE & ADMINISTRATION

Directions Pump enough product on your palm to thoroughly cover your hands.

Rub together until dry.

Children under 6 years should be supervised when using this product.

INDICATIONS & USAGE

Uses Hand Sanitizer to help reduce bacteria on the skin that could cause disease

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SINOFRESH FOAMING HAND SANITIZER 
foaming hand sanitizer aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79961-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.12 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79961-001-01	30000 mg in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	08/17/2020
2	NDC: 79961-001-02	50000 mg in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	08/17/2020
3	NDC: 79961-001-03	207000 mg in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	08/17/2020
4	NDC: 79961-001-04	3800000 mg in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	08/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/17/2020

Labeler - ZapVir, Inc. (117600850)

Registrant - ZapVir, Inc. (117600850)