NDC 66096-117 Ohm-detl

Boldo, Carduus Marianus, Chelidonium Majus, China Officinalis, Cynara Scolymus, Hydrastis Canadensis, Nux Vomica, Stannum Metallicum, Taraxacum Officinale

NDC Product Code 66096-117

NDC Code: 66096-117

Proprietary Name: Ohm-detl 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.

Non-Proprietary Name: Boldo, Carduus Marianus, Chelidonium Majus, China Officinalis, Cynara Scolymus, Hydrastis Canadensis, Nux Vomica, Stannum Metallicum, Taraxacum Officinale 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.

NDC Code Structure

  • 66096 - Ohm Pharma Inc.
    • 66096-117 - Ohm-detl

NDC 66096-117-02

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Ohm-detl with NDC 66096-117 is a a human over the counter drug product labeled by Ohm Pharma Inc.. The generic name of Ohm-detl is boldo, carduus marianus, chelidonium majus, china officinalis, cynara scolymus, hydrastis canadensis, nux vomica, stannum metallicum, taraxacum officinale. The product's dosage form is spray and is administered via oral form.

Labeler Name: Ohm Pharma Inc.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Ohm-detl Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • MILK THISTLE 5 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • TIN 16 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)

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.

Labeler Name: Ohm Pharma Inc.
Labeler Code: 66096
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 01-01-2010 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: 12-31-2019 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Ohm-detl Product Label Images

Ohm-detl Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTS (HPUS) - equal amounts of: Boldo 5X, Carduus Marianus 5X, Chelidonium Majus 5X, China Officinalis 7X, Cynara Scolymus 5X, Hydrastis Canadensis 5X, Nux Vomica 7X, Stannum Metallicum 16X, Taraxacum Officinale 5X.

Indications & Usage

Venta bajo prescriptión medica.


Medicamento Homeopatico.

Otc - Keep Out Of Reach Of Children

Mantengase fuera del alcance de los niños.

Dosage & Administration

DIRECTIONS: Shake 10 times before use. Spray 3 times under the tongue 2-3 times a day or as directed by health care professional. Children under 12: use half the adult dose.

Other Safety Information

Manufactured according to HPUS standards.CONDICIONES DE ALMACENAMIENTO: Conservar el producto protegido del calor, luz y humedad. Alcamacenat a no mas de 30C.

Inactive Ingredient


Otc - Questions

Mfg. By: OHM PHARMA INC.Mineral Wells, TX 76067R.S. INVIMA: MH2010-0001591Importado y Distribuido para Colombia por:OHM PHARMA COLOMBIA Ltda.DG. 39 NO 34 C SUR 30Envigado, AntioquiaTel: (57) 4-379 5995

Otc - Purpose

Temporarily relieves slow dysfunctional hepatic metabolism, stimulates liver function to remove toxins and improve drainage.

* Please review the disclaimer below.

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