ZEP ACCLAIM AB- benzalkonium chloride liquid 
Zep Inc.

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66949-131 / 3149 Acclaim AB

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic Hand Wash

Uses

Hand washing to decrease bacteria on skin.

Warnings

For external use only.

Do not use

Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

When using this product

Stop use and ask a doctor

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

Keep out of reach of children

Keep out of reach of children except under adult supervision.

Directions

Other Information

Inactive Ingredients

Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Cocamide DIPA, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Fragrance, Yellow 5, Red 4

Questions or comments?

Call 1-877-BUY-ZEP (1-877-428-9937)

131_3149

ZEP ACCLAIM AB 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-131
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
EDETATE SODIUM (UNII: MP1J8420LU)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-131-0111400 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
2NDC:66949-131-166000 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
3NDC:66949-131-116000 mL in 1 CASE; Type 0: Not a Combination Product12/15/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)12/15/2016
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.112125310manufacture(66949-131)

Revised: 10/2023
Document Id: 07ea9a37-7d58-8b08-e063-6394a90a3e21
Set id: b43bc291-bf12-fea6-e053-2a95a90aa74a
Version: 4
Effective Time: 20231020
 
Zep Inc.