66949-121 / 0900 Alcohol Sanitizer

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.

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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66949-121 / 0900 Alcohol Sanitizer

Active ingredient

Ethanol 73% 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

• Wet hands thoroughly with spray mist.
• Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles.
• Continue rubbing vigorously until hands are dry.
• No rinsing or toweling is required.

Other information

Store at 20 to 25°C (68 to 77°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: 66949-121
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 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: 66949-121-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	08/07/2000	12/31/2021
2	NDC: 66949-121-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	08/07/2000	12/31/2021
3	NDC: 66949-121-89	1040988 mL in 1 CONTAINER; Type 0: Not a Combination Product	08/07/2000	12/31/2021
4	NDC: 66949-121-01	11400 mL in 1 CASE; Type 0: Not a Combination Product	08/07/2000	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/07/2000	12/31/2021

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-121)

Revised: 1/2021

Document Id: b932a59c-a73a-5441-e053-2a95a90a4cfa

34390-5

Set id: b43cc65b-944d-1c20-e053-2995a90abcf7

Version: 2

Effective Time: 20210118