EPI-CLENZ INSTANT HAND ANTISEPTIC- ethyl alcohol aerosol, foam

Epi-Clenz Instant Hand Antiseptic by

Drug Labeling and Warnings

Epi-Clenz Instant Hand Antiseptic by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Uses

• For handwashing to decrease bacteria on skin that could cause disease.
• Recommended for repeated use

Warnings

For external use only - Hands

Flammable, keep away from fire, flame, heat sparks and sources of static discharge.

Contents under pressure. Do not store at temperatures above 120 F (48 C).

Do not puncture or incinerate.

Do not use

• in the eyes. In case of eye contact, immediately flush with water.
• on broken skin.
• Do not inhale or ingest.

Stop use and ask a doctor if

• irritation or redness develop
• condition persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands thoroughly with product
• rub hands together covering all surfaces until hands are dry
• children under 6 years of age should be supervised when using this product

Inactive ingredients

Aloe barbadensis gel, cetearyl alcohol, cetearyl glucoside, denatonium benzoate, emulsifying wax NF, hydrofluorocarbon 152A, isobutane, propane, propylene glycol, sodium benzoate, ter-butyl alcohol, water.

Other Information

Store below 110 F (43 C)

May discolor certain fabrics or surfaces

Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

EPI-CLENZ INSTANT HAND ANTISEPTIC 
ethyl alcohol aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-970
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
ISOBUTANE (UNII: BXR49TP611)
PROPANE (UNII: T75W9911L6)
WATER (UNII: 059QF0KO0R)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-970-12	44 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/07/2017
2	NDC: 53329-970-08	237 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/07/2017
3	NDC: 53329-970-06	473 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/07/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/30/2005

Labeler - Medline Industries, Inc. (025460908)