66949-134 / R462 Zep Hand Sanitizer

Zep Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP HAND SANITIZER- ethanol 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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66949-134 / R462 Zep Hand Sanitizer

Active ingredient

Ethanol 70% v/v

Purpose

Antiseptic

Uses

• Hand sanitizing to decrease bacteria on skin.
• No rinsing required.

Warnings

For external use only.

Flammable. Keep away from fire, flame or spark.

When using this product

• Avoid eye contact.
• If in eyes, rinse promptly and thoroughly with water.

Stop use and ask a doctor

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

Keep out of reach of children and pets

Keep out of reach of children and pets. Children must be supervised in use of this product.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Apply sanitizer spray.
• Rub the spray over hands and let dry.
• No rinsing or toweling is required.

Other information

• Store at 4 to 27°C (40 to 80°F).
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Deionized Water, Glycerin

Questions or comments?

Call 1-800-I-BUY-ZEP (1-800-428-9937)

ZEP HAND SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-134
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-134-10	11400 mL in 1 CASE; Type 0: Not a Combination Product	03/23/2020	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020	12/31/2023

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-134)

Revised: 12/2022

Document Id: f033be84-553f-36f2-e053-2a95a90a4d32

34390-5

Set id: b932c99e-697e-0955-e053-2995a90a853d

Version: 3

Effective Time: 20221219