WET WIPES- benzalkonium wipes cloth

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Hangzhou Beitai Daily Commodity Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

Do not use in the eyes

Stop use and ask a doctor if
irritation and redness develop
condition persists for, more than 72 hours

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

Do not use

Do not use in the eyes

WHEN USING

Stop use and ask a doctor if
irritation and redness develop
condition persists for, more than 72 hours

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
condition persists for, more than 72 hours

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

wet hands thoroughly with product and allow to dry without wiping

Other information

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Inactive ingredients

Water, glycerin, propylene glycol, EDTA disodium salt, phenoxyethanol, aloe vera leaf juice, tocopheryl acetate.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

WET WIPES 
benzalkonium wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77765-015
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77765-015-01	35 in 1 DRUM; Type 0: Not a Combination Product	09/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/12/2020

Labeler - Hangzhou Beitai Daily Commodity Co., Ltd. (412963380)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Beitai Daily Commodity Co., Ltd.		412963380	manufacture(77765-015)