ZEP ACCLAIM AB- benzalkonium chloride liquid 
ZEP PROFESSIONAL MILD AB- benzalkonium chloride liquid 
ZEP MILD ANTIBACTERIAL- benzalkonium chloride liquid 
Zep 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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66949-314/399/461 Acclaim AB

Benzalkonium Chloride 0.13%

Antiseptic Hand Wash

Uses

Hand washing to decrease bacteria on skin.

For external use only.

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

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

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

Keep out of reach of children except under adult supervision.

Directions

  • Wet hands with water.
  • Place hands under dispenser and apply liquid soap.
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.

Other Information

  • Store at room temperature.
  • Do not freeze.
  • Dispose in accordance with all applicable federal, state, and local regulations.

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)

3149 Acclaim AB

R399 R461

ZEP ACCLAIM AB 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-314
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:66949-314-2415140 mL in 1 CASE; Type 0: Not a Combination Product12/15/201612/31/2020
2NDC:66949-314-0111400 mL in 1 CASE; Type 0: Not a Combination Product12/15/201612/31/2020
3NDC:66949-314-16500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/15/201612/31/2020
4NDC:66949-314-116000 mL in 1 CASE; Type 0: Not a Combination Product12/15/201612/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/15/201612/31/2020
ZEP PROFESSIONAL MILD AB 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-399
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
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
GLYCERIN (UNII: PDC6A3C0OX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
EDETATE SODIUM (UNII: MP1J8420LU)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-399-06500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/201612/31/2020
2NDC:66949-399-253785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/10/201612/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/10/201612/31/2020
ZEP MILD ANTIBACTERIAL 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-461
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
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
EDETATE SODIUM (UNII: MP1J8420LU)  
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-461-2415140 mL in 1 CASE; Type 0: Not a Combination Product03/23/202012/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/23/202012/31/2020
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.112125310manufacture(66949-399, 66949-314, 66949-461)

Revised: 11/2020
 
Zep Inc.