ZEP BLUE SKY AB- benzalkonium chloride liquid

Zep Blue Sky AB by

Drug Labeling and Warnings

Zep Blue Sky AB by is a Otc medication manufactured, distributed, or labeled by Zep Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 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

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

• 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.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

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)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP BLUE SKY AB 
benzalkonium chloride liquid

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

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

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-332-11	6000 mL in 1 BOX; Type 0: Not a Combination Product	01/23/2017
2	NDC: 66949-332-24	15141 mL in 1 BOX; Type 0: Not a Combination Product	01/23/2017

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

Labeler - Zep Inc. (030471374)

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