HAND SANITIZER GEL- ethanol liquid

Hand Sanitizer Gel by

Drug Labeling and Warnings

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 bacteria that can potentially cause disease

■ For use when soap and water are not available

Warnings

For external use only.

Flammable. Keep away from source of heat or fire

Do Not Use

■ on children less than 2 months of age

■ on open skin wounds

■ on broken or damaged skin

When using this product

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or redness develops and lasts.

Keep out of reach of children and pets

Keep out of reach of children and pets. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

■ For occasional and personal use.

■ Rub thoroughly into hands for at least 30 seconds. Allow to dry.

■ Children under 6 years should be supervised when using this product.

Other information

■ store at a temperature below 110 °F (43 °C).

■ may discolor certain fabrics or surfaces.

Inactive ingredients

Water, Triisopropanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopheryl Acetate.

Questions?

1-800-514-6729

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER GEL 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-137
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
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-137-28	15140 mL in 1 CASE; Type 0: Not a Combination Product	07/05/2021
2	NDC: 66949-137-08	2840 mL in 1 CASE; Type 0: Not a Combination Product	07/05/2021	12/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/05/2021

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-137)