ZEP BLUE SKY AB- benzalkonium chloride liquid 
Zep Inc.

----------

66949-124 / 3321 Blue Sky AB Foam

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic Handwash

Uses

Hand washing to decrease bacteria on skin.

Warnings

For external use only.

Do not use

Do not use in or around 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, Di-PPG-2 Myreth-10 Adipate, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol, Tetrasodium Iminodisuccinate, Fragrance, Methylchloroisothiazolinone, Citric Acid, Blue 1

Questions or comments?

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

124_3321

ZEP BLUE SKY AB 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-124
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)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)  
HEXANEDIOL (UNII: ZIA319275I)  
TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66949-124-116000 mL in 1 CASE; Type 0: Not a Combination Product01/23/201712/31/2024
2NDC:66949-124-2415140 mL in 1 CASE; Type 0: Not a Combination Product01/23/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)01/23/2017
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIBusiness Operations
Zep Inc.112125310manufacture(66949-124)

Revised: 10/2023
Document Id: 07ea6a8d-4037-0c5e-e063-6294a90a4a6e
Set id: b4643941-bb50-a3bb-e053-2995a90a5c16
Version: 4
Effective Time: 20231020
 
Zep Inc.