Epi-Clenz Plus Instant Hand Antiseptic by Medline Industries, Inc. Drug Facts

Epi-Clenz Plus Instant Hand Antiseptic by

Drug Labeling and Warnings

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

Drug Details [pdf]

EPI-CLENZ PLUS INSTANT HAND ANTISEPTIC- ethyl alcohol lotion 
Medline Industries, 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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Drug Facts

Active ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on skin
  • recommended for repeated use.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

  • in the eyes. In case of eye contact, immediately flush with water.

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.

Inactive ingredients

Acrylates/ C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, C10-30 cholesterol/lanosterol esters, cetearyl alcohol, dimethicone, glycerin, isopropyl myristate, propylene glycol, simmondsia chinensis (jojoba) oil, styrene/acrylates copolymer, tocopheryl acetate, triethanolamine, water.

Package/Label Principal Display Panel

Epi-Clenz Instant Hand Antiseptic

NDC: 53329-208-20

PROFESSIONAL

Hand Hygiene

EPI-CLENZ Plus

INSTANT HAND ANTISEPTIC 

Latex Free

REF MSC097028

  • 62% v/v Ethyl Alcohol
  • With Added Moisturizers for Soft Feeling Hands

Medline

Vitamin E & Aloe Vera

24 FL OZ (800 mL)

EPI-CLENZ PLUS INSTANT HAND ANTISEPTIC 
ethyl alcohol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 53329-208
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
JOJOBA OIL (UNII: 724GKU717M)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 53329-208-1244.4 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/200710/23/2018
2NDC: 53329-208-201 in 1 BOX09/20/200710/23/2018
2800 mL in 1 BAG; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/20/200710/23/2018
Labeler - Medline Industries, Inc. (025460908)

Revised: 11/2019
Document Id: 982dd6e8-3d90-ad3c-e053-2995a90aa53d
Set id: d645ab34-1a96-48d1-b9d2-e2dd9e614f78
Version: 4
Effective Time: 20191125