Label: PROVE ALCOHOL PREP PADS- 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 March 30, 2020

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

  • Drug Facts

  • Active Ingredients

    Isopropyl Alcohol, 70% v/v

  • Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Use: For preparation of the skin prior to injection: to decrease germs in minor cuts and scrapes.

  • WARNINGS

    Warnings: For external use only. Flammable; keep away from the fire and flame.

    Caution: Do not apply to irritated skin.

    Do not use in the eyes or on mucous membranes.

    In case of deep or puncture wounds, consult a doctor.

    Keep out of reach of children.

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

  • DOSAGE & ADMINISTRATION

    Directions: Wipe injection site vigorously.

  • STORAGE AND HANDLING

    Other information: Store at room temperature.

  • INACTIVE INGREDIENT

    Inactive ingredients: Water

  • SPL UNCLASSIFIED SECTION

    70% Isopropyl alcohol for optimum anti-bacterial action


    Use as antiseptic for preparation of skin prior to injection


    Four-layer wrapper provides air-tight seal prevents leakage and drying out


    Manufactured In China For Future Brands

    PROVE is a Trademark of Future Brands

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    PROVE ALCOHOL PREP PADS 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70393-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70393-003-46200 in 1 BOX11/07/2019
    11 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/07/2019
    Labeler - Future Diagnostics Llc (080113296)