Label: MIRACLE WATER 3 IN 1- potassium hydroxide spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated July 9, 2020

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

View All Sections
  • Active Ingredients

    Potassium hydroxide

  • Purpose

    Cleaner, Disinfectant & Deodorization

  • Warnings

    Avoid eye contact. If product gets in eyes, just flush with water 

    Do not drink the product.

    If swallowed, drink as much of the drinking water as possible to neutralize alkaline water of the product, and go to the nearest medical hospital 

    Wear rubber glove if needed

  • Uses

    cleaning, disinfection, deodorization

  • Direction

    surface should be dry before spray.

    Apply evenly to the surface and allow the product to spray for about 10-20 seconds, then wipe it clean with dry cloth or towel.

    Product can be applied to fabric, furnishings, tile, ceramic, glass, stainless steel& pet supplies etc.

  • Keep out of reach of childrens

  • SPL UNCLASSIFIED SECTION

    Store in a cool, dry place away from heat and direct sunlight. 

    The efficacy of the product lasts for about six months maximum after opening.

    Recycle the empty container. 

    Dispose following local regulations or Safe for drain disposal.

  • Inactive Ingredients

    Water

  • Product Label

    image description

  • INGREDIENTS AND APPEARANCE
    MIRACLE WATER 3 IN 1 
    potassium hydroxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79659-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) (HYDROXIDE ION - UNII:9159UV381P) POTASSIUM HYDROXIDE0.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79659-001-01400 mL in 1 PACKAGE; Type 0: Not a Combination Product07/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/16/2020
    Labeler - ORIGIN G&B CO.,LTD (694822108)
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!