Zep Aspen by Zep Inc. Zep Aspen

Zep Aspen by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP ASPEN- 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 Aspen

Active ingredient

Triclosan 0.1%

Purpose

Antimicrobial

Uses

Hand washing to decrease bacteria on 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 contact 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

• Wet hands with water
• Place hands under dispenser
• Apply foamed 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.

Inactive ingredients

Water, Sodium Lauryl Sulfoacetate (and) Disodium Laurethsulfosuccinate, Sodium Cocoyl Sarcosinate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerine, Hexylene Glycol, PEG-75 Lanolin, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazoline, Fragrance, Glutaral

ZEP ASPEN 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-601
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 SULFOACETATE (UNII: D0Y70F2B9J)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
GLYCERIN (UNII: PDC6A3C0OX)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
PEG-75 LANOLIN (UNII: 09179OX7TB)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GLUTARAL (UNII: T3C89M417N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-601-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/14/2002	01/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/14/2002	01/01/2020

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		030471374	manufacture(66949-601)

Revised: 9/2017

Document Id: 5a06d162-6fcd-0d7c-e053-2991aa0a18f4

34390-5

Set id: 3f95cedf-d58b-4301-9c4b-7363c5da656f

Version: 6

Effective Time: 20170925

 

Zep Inc.