ZEP INSTANT HAND SANITIZER GEL- alcohol liquid

Zep Instant Hand Sanitizer Gel by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Ethanol 70% v/v

Purpose

Antiseptic

Uses

■ To help reduce germs and bacteria on the 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 quantities 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 use of this product.

Directions

• Apply gel to hands.
• Rub into hands for at least 20 seconds or until dry.

Other information

■ Keep container closed and stored in a dry area at temperatures between 68°F and 77°F (20°C and 25°C).
■ 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 1-877-I-BUY-ZEP (1-877-428-9937)

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ZEP INSTANT HAND SANITIZER GEL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-118
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)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-118-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	09/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/28/2020

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-118)