ZEP APPLAUD AB- chloroxylenol liquid

Zep Applaud AB by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Chloroxylenol 0.3%

PURPOSE

Antiseptic

Uses

Hand washing to decrease bacteria on skin.

For external use only.

• For external use only.

Do not use

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

When using this product

• 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.

WARNINGS

Stop use 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 liquid soap.
• Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.
• Rinse thoroughly.

Other information

• Store at room temperature.
• Do not freeze.
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Water, Potassium Tallate, Cocamide DIPA, Lauric Acid, Sodium Chloride, Tetrasodium EDTA, Acrylates/PEG-10 maleate/Styrene Copolymer, Isopropyl Alcohol, Fragrance, BHT, Red 4, Red 33

Questions or comments?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP APPLAUD AB 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-385
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
POTASSIUM LAURATE (UNII: V4361R8N4Z)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
EDETATE SODIUM (UNII: MP1J8420LU)
METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-385-01	11400 mL in 1 CONTAINER; Type 0: Not a Combination Product	03/10/2017
2	NDC: 66949-385-24	15140 mL in 1 CONTAINER; Type 0: Not a Combination Product	03/10/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/10/2017

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-385)