ZEP BLUE SKY AB- 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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66949-332 Blue Sky AB Foam

Benzalkonium Chloride 0.13%

Antiseptic Hand Wash

Uses

Hand washing to decrease bacteria on skin.

For external use only.

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

When using this product

Do not swallow.
If swallowed, 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.
Apply foamed soap.
Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.
Rinse hands thoroughly and dry.

Store at 20 to 25°C (68 to 77°F).
Do not freeze.
Dispose in accordance with all applicable federal, state and local regulations.

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)

3321

ZEP BLUE SKY AB
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66949-332
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66949-332-11	6000 mL in 1 BOX; Type 0: Not a Combination Product	01/23/2017	12/31/2020
2	NDC:66949-332-24	15141 mL in 1 BOX; Type 0: Not a Combination Product	01/23/2017	12/31/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/23/2017	12/31/2020

Labeler - Zep Inc. (030471374)

Name	Address	ID/FEI	Business Operations
Establishment
Zep Inc.		112125310	manufacture(66949-332)

Revised: 11/2020

Document Id: b4643941-bb53-a3bb-e053-2995a90a5c16

Set id: 5bbf49af-1eae-3b6f-e053-2a91aa0a8fe4

Version: 4

Effective Time: 20201118

Zep Inc.