Zep Cherry Creme Hand Soap

Zep Cherry Creme by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP CHERRY CREME- 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 Cherry Creme Hand Soap

Active ingredient

Triclosan 0.1%

Purpose

Antimicrobial

Uses

For handwashing to decrease bacteria on skin.

Warnings

For external use only.

When using this product

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

Stop use and ask doctor if skin irritation develops.

Except under adult supervision,  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, Sodium Lauryl Sulfate, Cocomidopropyl Betaine, Cocamide DIPA, Glycol Stearate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Tetrasodium EDTA, Fragrance, Citric Acid, Methylchloroisothiazolinone (and) Methylisothiazolinone, Glutaral, Sodium Xylenesulfonate, Sodium Chloride, Red 4, Red 33

ZEP CHERRY CREME 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-898
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
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
GLYCOL STEARATE (UNII: 0324G66D0E)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
GLYCERIN (UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GLUTARAL (UNII: T3C89M417N)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-898-24	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2003	01/01/2020
2	NDC: 66949-898-00	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2003	01/01/2020
3	NDC: 66949-898-10	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/26/2003	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/26/2003	01/01/2020

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		030471374	manufacture(66949-898)

Revised: 9/2017

Document Id: 5a0760ea-1069-fd62-e053-2991aa0a4855

34390-5

Set id: 73a95e74-09ab-4b9f-9828-671b23edfb0f

Version: 6

Effective Time: 20170925

 

Zep Inc.