AFCO 5511 SANIFECT E3- ethanol liquid

AFCO 5511 Sanifect E3 by

Drug Labeling and Warnings

AFCO 5511 Sanifect E3 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

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

Warnings

For external use only.
Do not usein 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 ifskin 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 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)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AFCO 5511 SANIFECT E3 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-140
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: 66949-140-01	208198 mL in 1 DRUM; Type 0: Not a Combination Product	05/05/2025
2	NDC: 66949-140-02	6000 mL in 1 CASE; Type 0: Not a Combination Product	05/05/2025
3	NDC: 66949-140-03	3785 mL in 1 CASE; Type 0: Not a Combination Product	05/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/05/2025

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-140)