NDC 59623-013 Mold Relief Formula
Kali Muriaticum, Gelsemium, Kali Bichromicum, Sabadilla, Histaminum, Mold Mix. Liquid Oral

Product Information

Mold Relief Formula is a human over the counter drug product labeled by Integrative Healing Institute, Llc. The generic name of Mold Relief Formula is kali muriaticum, gelsemium, kali bichromicum, sabadilla, histaminum, mold mix.. The product's dosage form is liquid and is administered via oral form.

Product Code59623-013
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Mold Relief Formula
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Kali Muriaticum, Gelsemium, Kali Bichromicum, Sabadilla, Histaminum, Mold Mix.
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Integrative Healing Institute, Llc
Labeler Code59623
Marketing Category What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
NDC Code Structure

What are the uses for Mold Relief Formula?

Product Packages

NDC 59623-013-01

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC 59623-013-02

Package Description: 59 mL in 1 BOTTLE, DROPPER

Product Details

What are Mold Relief Formula Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Mold Relief Formula Active Ingredients UNII Codes

Mold Relief Formula Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

Pharmacologic Class(es)

* Please review the disclaimer below.

Mold Relief Formula Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Otc - Active Ingredient

Active ingredients: Equal parts of: Kali Muriaticum 6X HPUS, Gelsemium 12C HPUS, Kali Bichromicum 12C HPUS, Sabadilla 12C HPUS, Histaminum 30C HPUS, Mold Mix 12X, 30X, 60X.*

Otc - Purpose

Purpose: Relief from runny nose, itchy eyes, sinus congestion and sneezing.

Indications & Usage

Use: This product is a Homeopathic Dilution, formulated to support the body's immunity for the temporary relief of mold allergies.



  • Use only as directed.
  • Stop use and consult a doctor if symptoms worsen or do not improve after 5 days.
  • If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

Directions:Shake bottle well before use.

  • Adults (12 and Older) Take 6-10 drops orally (in water if desired) 1-3 times a day as needed.
  • Children (11 and Younger) Take 4-6 drops orally (in water if desired) 1-3 times a day as needed or as directed by your health care provider.
  • Consult a Physician for use in children under 12 years of age.

Other Safety Information

Other information: Do not use if TAMPER EVIDENT seal around neck is broken or missing.
  • Store at room temperature.
  • * For a complete list of Mold antigens included in this product visit our website.

    Mfg. by: OHM Pharma, Inc., Mineral Wells, TX 76067
    Made in USA


Inactive Ingredient

Inactive ingredients: Citric Acid, Potassium Sorbate, Purified Water.

Otc - Questions


San Antonio, TX 78216
Questions? Call 1.888.841.4034

Package Label.Principal Display Panel



  • NDC: 59623-013-01   


    • SAFE
      • NET 1 fl oz (30 mL)

* Please review the disclaimer below.