Label: IODO ALBO IODIDE- alcohol liquid liquid

  • 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 9, 2020

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

View All Sections
  • DOSAGE & ADMINISTRATION

    Clean the affected area, apply a small amount on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

  • ACTIVE INGREDIENT

    Ethyl Alcohol 48%

  • INDICATIONS & USAGE

    First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns.

  • WARNINGS

    For External Use Only.

    When using this product:

    Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately. Soap will deactivate the effects of this product.

  • INACTIVE INGREDIENT

    • Ammonium Hydroxide
    • Iodine
    • Potassium Iodide
    • Purified Water
  • PURPOSE

    First Aid Antiseptic

  • Iodo Albo Iodide

    Iodo Albo Iodides.jpg

  • INGREDIENTS AND APPEARANCE
    IODO ALBO IODIDE 
    alcohol liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53145-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.48 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    IODINE (UNII: 9679TC07X4)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    AMMONIA (UNII: 5138Q19F1X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53145-120-9130 mL in 1 CONTAINER; Type 0: Not a Combination Product04/09/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/09/2019
    Labeler - Menper Distributors Inc. (101947166)
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!