WET WIPES- benzalkonium chloride swab

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 0.1%

Purpose

Antiseptic

Uses

decreases bacteria on the skin

Warnings

For external use only

Do not use

Over large areas of the body 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

Stop use and ask a doctor if irritation or rash develops and continues 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

  for adults and children 2 years and over use on hands and face to clean and refresh, allow skin to air dry.  For children under 2 years of age ask a doctor before use.

Inactive Ingredients

water, propylene glycol, cocamidopropyl betaine, peg-7 glyceryl cocoate, fragrance, benzyl alcohol, methylchloroisothiazolinine, methylisothiazolinone, tetrasodium EDTA, peg-40 hydrogenated castor oil, cetrimonium chloride, citric acid, aloe vera extract, alphatocopherol acetate

Package Label

INGREDIENTS AND APPEARANCE

WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-431
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
EDETATE SODIUM (UNII: MP1J8420LU)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-431-30	30 in 1 PACKAGE; Type 0: Not a Combination Product	01/23/2007
2	NDC: 20276-431-36	36 in 1 PACKAGE; Type 0: Not a Combination Product	01/23/2007
3	NDC: 20276-431-40	40 in 1 PACKAGE; Type 0: Not a Combination Product	06/06/2016
4	NDC: 20276-431-16	16 in 1 PACKAGE; Type 0: Not a Combination Product	06/06/2016
5	NDC: 20276-431-80	80 in 1 PACKAGE; Type 0: Not a Combination Product	10/04/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/23/2007

Labeler - Delta Brands, Inc (102672008)