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Name:Alcohol Prep
Manufacturer:Chain Drug Consortium, Llc
Category:Over-the-counter (OTC) Marketed Drugs


Alcohol Prep Pad

ALCOHOL PREP  - isopropyl alcohol swab 
Chain Drug Consortium, LLC

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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Alcohol Prep Pad

Active Ingredient                                       Purpose

Isopropyl Alcohol 70% v/v                         Antiseptic


Use:alcohol prep

For preparation of the skin prior to injection.

Warnings:

  • For external use only
  • Flammable, keep away from flame or fire
  • Not for use with electrocautinary devices or procedures
  • Do not use in eyes

Indications and Usage:

Stop use and ask a doctor if:

  • Irritation or redness develops
  • condition persists for more than 72 hours
  • Cleansing of an injection site

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Directions:

Wipe injection site vigorously and discard

Other information:

  • Store at room temperature: 15 deg C to 30 deg C   59 deg F to 86 deg F
  • avoid excessive heat

Inactive Ingredient

Inactive Ingredient

  • Water

Principal Display Panel

alcohol_prep

alcohol_prep


ALCOHOL PREP 
isopropyl alcohol swab
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-012
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 1.4 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68016-012-90 10 BOX ( BOX) in 1 CASE contains a BOX
1 100 SWAB ( SWAB) in 1 BOX This package is contained within the CASE (68016-012-90)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 04/21/2011

Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 05/2011 Chain Drug Consortium, LLC



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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