Zep Lemongrass by Zep Inc. Zep Lemongrass Hand Soap

Zep Lemongrass by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP LEMONGRASS- 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 Lemongrass Hand Soap

Active Ingredients

Triclosan 0.1%

Purpose

Antimicrobial

Uses

• For handwashing to decrease bacteria on the skin.

Warnings

For external use only.
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.

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

Keep out of reach of children except under adult supervision.

Directions

Press pump to dispense product onto hands, lather and rinse.

Other information

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

Inactive Ingedients

water, sodium lauryl sulfate, cocamidopropyl betaine, cocamide DIPA, Cocamidopropyl PG-Dimonium Chloride Phosphateglycerin, citric acid, glycerin, tetrasodium EDTA, fragrance, Sodium Chloride, Methylchloroisothiazolinone (and) Methylisothiazolinone, Glutural, Sodium Xylenesulfonate, Yellow 5, Blue 1

ZEP LEMONGRASS 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-882
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
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GLUTARAL (UNII: T3C89M417N)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
WATER (UNII: 059QF0KO0R)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-882-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2013	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2012	01/01/2020

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		030471374	manufacture(66949-882)

Revised: 11/2016

Document Id: 40414a57-cb7b-087b-e054-00144ff88e88

Set id: 2f6e6d6a-0fd2-3db5-e054-00144ff8d46c

Version: 2

Effective Time: 20161101

 

Zep Inc.