Drug Facts

Drug Facts

Drug Labeling and Warnings

Drug Details

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WET WIPES- benzalkonium chloride swab 
Delta Brands, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

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

Package Label

WET WIPES 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 20276-431
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 20276-431-3030 in 1 PACKAGE; Type 0: Not a Combination Product01/23/2007
2NDC: 20276-431-3636 in 1 PACKAGE; Type 0: Not a Combination Product01/23/2007
3NDC: 20276-431-4040 in 1 PACKAGE; Type 0: Not a Combination Product06/06/2016
4NDC: 20276-431-1616 in 1 PACKAGE; Type 0: Not a Combination Product06/06/2016
5NDC: 20276-431-8080 in 1 PACKAGE; Type 0: Not a Combination Product10/04/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/23/2007
Labeler - Delta Brands, Inc (102672008)

Revised: 1/2020
 
Delta Brands, Inc


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