Zep Lemongrass

Manufacturer: Zep Inc.
Effective date: 2016-11-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 01:21:58

Label at a glance#

ProductZep Lemongrass

Active ingredientTRICLOSAN

Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Triclosan 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

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

When using this Product

OTC - WHEN USING SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

OTHER SAFETY INFORMATION

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

Inactive Ingedients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0882

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

Zep Lemongrass
Triclosan
COCAMIDOPROPYL BETAINE
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
FD&C BLUE NO. 1
ANHYDROUS CITRIC ACID
GLYCERIN
SODIUM CHLORIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
GLUTARAL
FD&C YELLOW NO. 5
WATER
SODIUM LAURYL SULFATE
SODIUM XYLENESULFONATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
66949-882	66949-882-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
TRICLOSAN	4NM5039Y5X	ACTIB
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
GLUTARAL	T3C89M417N	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
WATER	059QF0KO0R	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SODIUM XYLENESULFONATE	G4LZF950UR	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
40414a57-cb7b-087b-e054-00144ff88e88			2f6e6d6a-0fd2-3db5-e054-00144ff8d46c	2016-11-01	Warnings	Exact identifier spl id: 40414a57-cb7b-087b-e054-00144ff88e88 spl set id: 2f6e6d6a-0fd2-3db5-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.