NDC 50845-0256 Antacid

Anacardium Orientale, Argentum Nitricum, Bismuthum Metallicum, Condurango, Geranium Maculatum, Nux Vomica, Phosphorus, Pyrogenium, Robinia Pseudoacacia, Sulphuricum Acidum

NDC Product Code 50845-0256

NDC Code: 50845-0256

Proprietary Name: Antacid 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: Anacardium Orientale, Argentum Nitricum, Bismuthum Metallicum, Condurango, Geranium Maculatum, Nux Vomica, Phosphorus, Pyrogenium, Robinia Pseudoacacia, Sulphuricum Acidum 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

  • 50845 - Liddell Laboratories, Inc.
    • 50845-0256 - Antacid

NDC 50845-0256-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Antacid with NDC 50845-0256 is a a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Antacid is anacardium orientale, argentum nitricum, bismuthum metallicum, condurango, geranium maculatum, nux vomica, phosphorus, pyrogenium, robinia pseudoacacia, sulphuricum acidum. The product's dosage form is spray and is administered via oral form.

Labeler Name: Liddell Laboratories, 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.

Antacid 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.

  • SEMECARPUS ANACARDIUM JUICE 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • BISMUTH 30 [hp_C]/mL
  • MARSDENIA CONDURANGO BARK 200 [hp_C]/mL
  • GERANIUM MACULATUM ROOT 3 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • RANCID BEEF 30 [hp_C]/mL
  • ROBINIA PSEUDOACACIA BARK 6 [hp_X]/mL
  • SULFURIC ACID 6 [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.

  • WATER (UNII: 059QF0KO0R)
  • 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: Liddell Laboratories, Inc.
Labeler Code: 50845
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: 07-11-2019 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: 12-31-2020 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.

Antacid Product Label Images

Antacid 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

Active Ingredients:

(in each spray) 10% of Anacardium Orientale 6X, Argentum Nitricum 6X, Bismuthum Metallicum 30C, Condurango 200C, Geranium Maculatum 3X, Nux Vomica 6X, Phosphorus 12X, Pyrogenium 30C, Robinia Pseudoacacia 6X, Sulphuricum Acidum 6X.

Indications:

May temporarily relieve symptoms associated with heartburn & excess stomach acid: stomach pain, indigestion, nausea, bloating.**** These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

May temporarily relieve symptoms associated with heartburn & excess stomach acid: stomach pain, indigestion, nausea, bloating.**** These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If symptoms persist, consult a doctor.If pregnant or breast feeding, ask a doctor before use.Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Directions:

Adults and Children over 12: Spray twice under the tongue up to each 30 minutes until symptoms are relieved. As a preventative, spray twice under the tongue three times per day.Children 12 and under: Consult a doctor prior to use.

Inactive Ingredients:

Organic alcohol 20% v/v, Purified water.

Questions:

DIST. BY LIDDELL LABORATORIES, INC.WOODBINE, IA 51579WWW.LIDDELL.NET 1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELLLABORATORIESEST. 199412A-aAntacidHOMEOPATHIC1.0 FL. OZ. (30 ml)

* Please review the disclaimer below.

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