Label: VIAMED ALCOHOL PREP PAD- alcohol swab

  • NDC Code(s): 42947-500-01
  • Packager: Wuxi Medical Instrument Factory
  • 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 February 3, 2023

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

  • Drug facts

    Active Ingredient

    Isopropyl Alcohol 70%

    Purpose

    Antiseptic

  • Use

    For preparation of skin prior to injection

  • Warnings

    For external use only. Flammable keep away from the fire or flame

    Do not use

    *with electrocautery procedures* in the eyes

    Stop use

    if irritation or redness develop. If your condition persists for more than 72 hours, consult a doctor.

    Keep out of the reach of children

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

  • Directions

    Wipe injectio site vigorously and discard after single use.

  • Inactive Ingredient

    Purified water

  • Product labeling

    ViaMed

    Alcohol Prep Pad

    For external use only

    One pad Saturated with 70% Isopropyl Alcohol

    Made in China

    Rece International Corp

    Miami Lakes, FL 33014

    label

    label2

  • INGREDIENTS AND APPEARANCE
    VIAMED ALCOHOL PREP PAD 
    alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42947-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42947-500-01100 in 1 PACKAGE09/10/2015
    10.36 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/10/2015
    Labeler - Wuxi Medical Instrument Factory (421292863)
    Registrant - Wuxi Medical Instrument Factory (421292863)