NDC 66096-706 Ohm Mucus Relief

Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali Muriaticum, Kali Sulphuricum, Marrubium Vulgare.

NDC Product Code 66096-706

NDC Code: 66096-706

Proprietary Name: Ohm Mucus Relief 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: Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali Muriaticum, Kali Sulphuricum, Marrubium Vulgare. 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.
    • 66096-706 - Ohm Mucus Relief

NDC 66096-706-23

Package Description: 186 TABLET, CHEWABLE in 1 BOTTLE

NDC Product Information

Ohm Mucus Relief with NDC 66096-706 is a a human over the counter drug product labeled by Ohm Pharma Inc.. The generic name of Ohm Mucus Relief is antimonium crudum, antimonium tartaricum, chelidonium majus, ferrum phosphoricum, kali carboonicum, kali muriaticum, kali sulphuricum, marrubium vulgare.. The product's dosage form is tablet, chewable and is administered via oral form.

Labeler Name: Ohm Pharma Inc.

Dosage Form: Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.

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 Mucus Relief 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.

  • ANTIMONY TRISULFIDE 6 [hp_C]/1
  • ANTIMONY POTASSIUM TARTRATE 6 [hp_C]/1
  • CHELIDONIUM MAJUS 6 [hp_X]/1
  • FERROSOFERRIC PHOSPHATE 6 [hp_X]/1
  • POTASSIUM DICHROMATE 12 [hp_X]/1
  • POTASSIUM CARBONATE 30 [hp_C]/1
  • POTASSIUM CHLORIDE 6 [hp_X]/1
  • POTASSIUM SULFATE 6 [hp_X]/1
  • MARRUBIUM VULGARE 9 [hp_C]/1

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.

  • DEXTROSE (UNII: IY9XDZ35W2)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

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: 05-14-2015 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’.

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Ohm Mucus Relief Product Label Images

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