ZEP TRANQ MDW AB FOAM- benzalkonium chloride liquid

Zep Tranq Mdw AB Foam by

Drug Labeling and Warnings

Zep Tranq Mdw AB Foam 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

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

• 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

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 and pets. Children must be supervised in use of this product.

Directions

• Wet hands with water.
• Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
• Rinse thoroughly and dry.

OTHER SAFETY INFORMATION

• Store at 20 to 25°C (68 to 77°F).
• 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, 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)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP TRANQ MDW AB FOAM 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-387
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
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-387-04	6000 mL in 1 CASE; Type 0: Not a Combination Product	08/02/2017
2	NDC: 66949-387-09	3300 mL in 1 CASE; Type 0: Not a Combination Product	08/02/2017
3	NDC: 66949-387-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	08/02/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/02/2017

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-387)