ZAPRO HAND SANITIZER- hand sanitizer gel

ZAPRO HAND SANITIZER by

Drug Labeling and Warnings

ZAPRO HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 94%

Purpose

Antiseptic

Use

Use
for hand washing to decrease bacteria on he skin， only when water is not ava able

Warnings

Flammable—Keep away from fire and flames
For external use only

Do not use

Do not get into eyes
lf contact occurs， rinse thoroughly with water

When using this product

When using this product
Do not get into eyes
lf contact occurs， rinse thoroughly with water

Stop use and ask a doctor if
Irritation and redness develop

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

STOP USE

Stop use and ask a doctor if
Irritation and redness develop

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

Press pump twice to dever two s quits of product on to the pam of your hand
Rub hands together and allow to dry without wiping

Other information

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

Inactive ingredients

water, cellulosico-polymer, zinc pyrithione

Package Label - Principal Display Panel

75209-011-01 250ml

75209-011-02 2000ml

INGREDIENTS AND APPEARANCE

ZAPRO HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75209-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	94 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5)
WATER (UNII: 059QF0KO0R)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75209-011-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/22/2020
2	NDC: 75209-011-02	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/22/2020

Labeler - GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD. (546631081)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.		546631081	manufacture(75209-011)