Zep Mango Foaming by Zep Inc. Zep Mango Hand Soap

Zep Mango Foaming by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP MANGO FOAMING- triclosan 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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Zep Mango Hand Soap

Active ingredient

Triclosan 0.1%

Purpose

Antiseptic Handwash

Uses

For handwashing to decrease bacteria on this skin.

Warnings

For external use only.

Do not use in the eyes.

When using this product

• if swallowed, seek medical attention.
• if eye contact occurs, flush eyes with water and consult a physician.

Discontinue use if irritation and redness develop.

If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

Directions

• press pump to dispense product onto hands, lather and rinse.

Other information

• Store at room temperature
• Do not freeze

Inactive ingredients

Water, Ammonium Lauryl Sulfate, Ammonium Laureth-3 Sulfate, Cocamide DIPA, Disodium Ricinoleic MEA Sulfosuccinate, Fragrance, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazolinone, Citric Acid, Glutaral, Yellow 5, Red 4

ZEP MANGO FOAMING 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-874
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.01 g  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
DISODIUM RICINOLEIC MONOETHANOLAMIDE SULFOSUCCINATE (UNII: 1YHW4GJC3U)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLUTARAL (UNII: T3C89M417N)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-874-00	550 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/16/2003	01/01/2020
2	NDC: 66949-874-15	2500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/16/2003	01/01/2020
3	NDC: 66949-874-10	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/16/2003	01/01/2020
4	NDC: 66949-874-01	550 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/16/2003	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/16/2003	01/01/2020

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		030471374	manufacture(66949-874)

Revised: 9/2017

Document Id: 5a07a11d-62c0-18a6-e053-2991aa0a0c1d

34390-5

Set id: 335cd6f3-d551-4dc7-a03a-fdda3f191fa6

Version: 6

Effective Time: 20170925

 

Zep Inc.