NDC 57955-5024 Indigestion Relief

Antimonium Crudum, Argentum Nitricum, Carbo Vegetabilis, Chelidonium Majus, Cinchona Officinalis, Graphites, Hydrastis Canadensis, Ipecacuanha, Kali Carbonicum, Lycopodium Clavatum, Nux Vomica, Pulsatilla

NDC Product Code 57955-5024

NDC Code: 57955-5024

Proprietary Name: Indigestion 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, Argentum Nitricum, Carbo Vegetabilis, Chelidonium Majus, Cinchona Officinalis, Graphites, Hydrastis Canadensis, Ipecacuanha, Kali Carbonicum, Lycopodium Clavatum, Nux Vomica, Pulsatilla 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

  • 57955 - King Bio Inc.
    • 57955-5024 - Indigestion Relief

NDC 57955-5024-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Product Information

Indigestion Relief with NDC 57955-5024 is a a human over the counter drug product labeled by King Bio Inc.. The generic name of Indigestion Relief is antimonium crudum, argentum nitricum, carbo vegetabilis, chelidonium majus, cinchona officinalis, graphites, hydrastis canadensis, ipecacuanha, kali carbonicum, lycopodium clavatum, nux vomica, pulsatilla. The product's dosage form is liquid and is administered via oral form.

Labeler Name: King Bio Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Indigestion 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.

  • SILVER NITRATE 10 [hp_X]/59mL
  • CHELIDONIUM MAJUS 10 [hp_X]/59mL
  • GRAPHITE 10 [hp_X]/59mL
  • GOLDENSEAL 10 [hp_X]/59mL
  • IPECAC 10 [hp_X]/59mL

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)

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: King Bio Inc.
Labeler Code: 57955
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: 05-05-2014 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: 12-31-2018 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: E 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.

Indigestion Relief Product Label Images

Indigestion Relief 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

Drug Facts​__________________________________________________________________________________________________________HPUS active ingredients: Antimonium crudum, Argentum nitricum, Carbo vegetabilis, Chelidonium majus, cinchona officinalis, Graphites, Hydrastis canadensis, Ipecacuanha, Kali carbonicum, Lycopodium clavatum, Nux vomica, Pulsatilla. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

Indications & Usage

Uses for temporary relief of symptoms following food or drink consumption: gas, bloating, belching, intestinal distress, hiccups, flatulence, sleepiness.

Inactive Ingredient

Inactive Ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.


  • WarningsStop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, ask a healthcare professional before use.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

  • DirectionsInitially, depress pump until primed.Spray one dose directly into mouth.Ages 12 and up: 3 sprays 3 times per day.Ages 2-12: 2 sprays 3 times per day

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact.

Otc - Purpose

  • Uses for temporary relief of symptoms following food or drink consumption: gasbloatingbelchingintestinal distresshiccupsflatulencesleepiness

* Please review the disclaimer below.

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