SANTIZALL 75 PERCENT ETHANOL WET WIPE- alcohol cloth

SantiZall 75 percent Ethanol Wet Wipe by

Drug Labeling and Warnings

SantiZall 75 percent Ethanol Wet Wipe by is a Otc medication manufactured, distributed, or labeled by Glory Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 75% v/v

INACTIVE INGREDIENTS

Water, Cetylpyridinium chloride, Glycerin, Polysorbate, Caprylhydroxamic acid, Citric acid

PURPOSE

ANTISEPTIC

WARNINGS

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Uses

Hand sanitizing wipes to help reduce bacteria that potentially can cause disease.

Directions

■ Wet hands thoroughly with product and allow to dry without wiping
■ Do not flush
■ Children under 2 years ask a doctor before use

Other information

■ Read the directions and warnings before use
■ Store between 15-30℃(59-89℉)
■ Avoid freezing and excessive heat above 40℃(104 ℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANTIZALL 75 PERCENT ETHANOL WET WIPE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78580-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75   in 100

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
Glycerin (UNII: PDC6A3C0OX)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78580-020-01	100 in 1 PACKET; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2020

Labeler - Glory Co., Ltd. (688492036)

Registrant - Glory Co., Ltd. (688492036)

Establishment
Name	Address	ID/FEI	Business Operations
Glory Co., Ltd.		688492036	manufacture(78580-020)