66949-135 / 0878 Instant Hand Sanitizer Gel

Zep Instant Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZEP INSTANT 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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66949-135 / 0878 Instant Hand Sanitizer Gel

Active Ingredient

Ethanol 67% v/v

Purpose

Antiseptic

Uses

• Hand sanitizing to decrease bacteria on skin.
• Recommended for repeated use.
• No rinsing required.

Warnings



• Flammable. Keep away from fire, flame or spark. For external use only.

. Do not use in the eye; if in eyes, rinse thoroughly with water.

When using this product

• Do not swallow.
• If swallowed, do not induce vomiting and if individual is conscious, give large quantity of water to drink and consult a physician immediately.

Stop use and ask doctor

Stop use and ask 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 the use of this product.

Directions

• Use pump and apply gel to hands.
• 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

• Keep container closed and stored in a dry area at temperatures between 4 to 27°C (40 to 80°F).
• Do not reuse empty container.
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Deionized Water, PEG-6 (and) Acrylates/Vinyl Crosspolymer, Fragrance.

Questions or comments?

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

ZEP INSTANT HAND SANITIZER 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-135
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-135-35	18927 mL in 1 PAIL; Type 0: Not a Combination Product	01/29/2004	12/31/2022
2	NDC: 66949-135-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	01/29/2004	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/29/2004	12/31/2022

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-135)

Revised: 1/2023

Document Id: f1ed709e-4da0-0f4d-e053-2995a90a2623

34390-5

Set id: be1172f3-f394-3213-e053-2995a90af316

Version: 3

Effective Time: 20230110