WET WIPES- benzalkonium chloride cloth

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Delta Brands, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Use

decreases bacteria on the skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients.

When using this product

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash develops and continues for more than 72 hours

Keep out of reach of children

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

Directions

adults and children ■ apply to hands

2 years and over ■ allow to dry

without wiping

children under ask a doctor

2 years before use

Inactive ingredients

water, propylene glycol, cocamidopropyl betaine,PEG-7 glyceryl cocoate, fragrance, phenylmethanol, methylchloroisothiazolinine, methylisothiazolinone, PEG-40 hydrogenated castor oil, tetrasodium EDTA, cetrimonium chloride, citric acid, tocopherol acetate

Package Label

INGREDIENTS AND APPEARANCE

WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-435
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
EDETATE SODIUM (UNII: MP1J8420LU)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-435-30	30 in 1 PACKAGE; Type 0: Not a Combination Product	05/18/2020
2	NDC: 20276-435-40	40 in 1 PACKAGE; Type 0: Not a Combination Product	05/18/2020
3	NDC: 20276-435-16	16 in 1 PACKAGE; Type 0: Not a Combination Product	05/18/2020
4	NDC: 20276-435-80	80 in 1 PACKAGE; Type 0: Not a Combination Product	05/18/2020
5	NDC: 20276-435-60	60 in 1 PACKAGE; Type 0: Not a Combination Product	05/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/18/2020

Labeler - Delta Brands, Inc (102672008)