Label: WALGREEN ALCOHOL- isopropyl alcohol swab

  • NDC Code(s): 0363-0809-30, 0363-0809-60, 0363-0809-67
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 12/13

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

  • Active ingredient

    Isopropyl alcohol, 70% v/v

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  • Purpose

    Antiseptic

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  • Uses

    for preparation of the skin prior to injection
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  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    Do not use

    with electrocautery procedures
    in the eyes

    Stop use and ask a doctor if

    irritation and redness develop
    condition persists for more than 72 hours

    Keep out of reach of children.

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

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  • Directions

    Wipe injection site vigorously and discard

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  • Other information

    Protect from freezing. Avoid excessive heat.

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  • Inactive ingredients

    Purified water

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  • Package/Label Principal Display Panel

    Walgreens Alcohol swab box, principal display panel and side

    Alcohol Prep Pads

    Isopropyl Alcohol 70%

    Antiseptic for preparation of the skin prior to injection

    200 INDIVIDUAL FOIL PACKETS

    STERILE

    200 Individual Foil Packets

    1.1 IN X 1.33 IN (2.8 cm x 3.4 cm)

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  • Package/Label Back
  • INGREDIENTS AND APPEARANCE
    WALGREEN ALCOHOL 
    isopropyl alcohol swab
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:0363-0809
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 70 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-0809-30 100 in 1 BOX
    1 1 in 1 PACKET
    1 5 mL in 1 APPLICATOR
    2 NDC:0363-0809-67 120 in 1 BOX
    2 1 in 1 PACKET
    2 5 mL in 1 APPLICATOR
    3 NDC:0363-0809-60 200 in 1 BOX
    3 1 in 1 PACKET
    3 5 mL in 1 APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/2011
    Labeler - Walgreen Company (008965063)
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