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Alcohol by MCL Enterprises

Medically reviewed on July 27, 2017

Dosage form: patch
Ingredients: ISOPROPYL ALCOHOL 700mg in 1g
Labeler: MCL Enterprises
NDC Code: 71622-004

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.

Alcohol Wipe

Drug Facts

Active Ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Use:

For preparation of the skin prior to injection.

Warnings:
  • For external use only
  • Flammable, keep away from fire or flame

Do not use:
  • longer than 1 week 
  • in the eyes

Stop use:
  • if irritation and redness develop. If condition persists consult a doctor.

Keep out of reach of children.

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

Directions:

Apply topically to cleanse the intended area and discard after single use.

Inactive Ingredient:

Purified Water

Package Labeling:

ALCOHOL 
isopropyl alcohol patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71622-004
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL700 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:71622-004-001 PATCH in 1 POUCH
10.42 g in 1 PATCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/25/2017
Labeler - MCL Enterprises (784754173)

 
MCL Enterprises

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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