Label: ALCOHOL PREP- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated July 8, 2014

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient                                       Purpose

    Isopropyl Alcohol 70% v/v                         Antiseptic


  • Purpose

    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
    • Sterile unless package is damaged or open.
  • 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 - box

    PRINCIPAL DISPLAY PANEL - 100 count box

    PAK-KIT FIRST AID

    STERILE ALCOHOL PREP PADS

    Contains 100 single use alcohol prep pads.

    See back panel for Drug Facts listing.

    Distributed by: Acme United Corporation

    Fairfield, CT 06824   800-835-2263

    PK alcohol prep B.jpg

    alcohol prep box

  • Principal Display Panel - packet

    PRINCIPAL DISPLAY PANEL - packet

    Dynarex Alcohol Prep Pad

    STERILE ALCOHOL PREP PADS


    Contains 1 single use alcohol prep pads.

    Acme United Corporation 

    Fairfield, CT 06824

    PK alcohol prep P.jpg

    alcohol prep packet

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-0011-06100 in 1 BOX
    10.55 mL in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/08/2014
    Labeler - Acme United Corporation (001180207)
    Registrant - Dynarex Corporation (008124539)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!