ZEP TRANQ MDW AB FOAM- benzalkonium chloride liquid 
Zep Inc.

----------

66949-387 / 3387 Tranquil Meadows AB

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial Hand Wash

Uses

For hand washing to decrease bacteria on skin.

Warnings

For external use only. 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 and pets

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

Other information

Inactive Ingredients

Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, Fragrance, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol, Tetrasodium Iminodisuccinate, Methylchloroisothiazolinone, Citric Acid, Blue 1, Yellow 5

Questions or comments?

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

387_3387

ZEP TRANQ MDW AB FOAM 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-387
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
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
HEXANEDIOL (UNII: ZIA319275I)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
WATER (UNII: 059QF0KO0R)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)  
TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-387-046000 mL in 1 CASE; Type 0: Not a Combination Product08/02/201712/31/2024
2NDC:66949-387-093300 mL in 1 CASE; Type 0: Not a Combination Product08/02/2017
3NDC:66949-387-2415140 mL in 1 CASE; Type 0: Not a Combination Product08/02/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)08/02/2017
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.112125310manufacture(66949-387)

Revised: 10/2023
Document Id: 07eaaf1b-1a86-b57d-e063-6294a90a3421
Set id: 5c3c1ab7-96a7-6ca5-e053-2991aa0af2b9
Version: 7
Effective Time: 20231020
 
Zep Inc.