66949-136 / 0900 / LHSS Alcohol Sanitizer Spray

Zep Alcohol Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP ALCOHOL SANITIZER- ethanol liquid 
Zep Inc.

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66949-136 / 0900 / LHSS Alcohol Sanitizer Spray

Active ingredient

Ethanol 70% v/v

Purpose

Antiseptic

Uses

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

Warnings

For external use only.
Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.
Flammable. Keep away from fire, flame or spark.

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

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.

Directions

• Apply santizer to hands.
• Rub into hands for at least 20 seconds or until 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; Glycerine

Questions or comments?

Call 1-877-I-BUY-ZEP (1-877-428-9937)

ZEP ALCOHOL SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-136
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-136-28	15140 mL in 1 CASE; Type 0: Not a Combination Product	03/22/2021	12/31/2024
2	NDC: 66949-136-32	11400 mL in 1 CASE; Type 0: Not a Combination Product	03/22/2021	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/22/2021	12/31/2024

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-136)

Revised: 10/2023

Document Id: 07eab1ff-e331-d278-e063-6394a90a4999

34390-5

Set id: be118e65-7924-ef60-e053-2a95a90a7608

Version: 4

Effective Time: 20231020