NDC 57955-0724 Grains And Gluten Intolerances

NDC Product Code 57955-0724

NDC 57955-0724-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Grains And Gluten Intolerances with NDC 57955-0724 is a product labeled by King Bio Inc.. The generic name of Grains And Gluten Intolerances is . The product's dosage form is and is administered via form.

Labeler Name: King Bio Inc.

Dosage Form: -

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.

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)

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
Start Marketing Date: 11-19-2013 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.

Grains And Gluten Intolerances Product Label Images

Grains And Gluten Intolerances 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: Arsenicum album, Bryonia, Histaminum hydrochloricum, Hydrastis canadensis, Lycopodium clavatum, Natrum muriaticum, Pulsatilla, Sabadilla, Secale cornutum, Sulphur. Equal volumes of each ingredient in 12X, 24X, LM1 potencies.

Indications & Usage

Uses temporarily relieves symptoms from grains and gluten intolerances and sensitivities: gas, heartburn, headache, nausea, or diarrhea.

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

  • Initially, depress pump until primed.​​Spray one dose directly into mouth.Ages 12 and up- 3 sprays 3 times per day.Ages 6-12- 2 sprays 3 times per day.

Other Safety Information

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

Otc - Purpose

  • Uses temporarily relieves symptoms from grains and gluten intolerances and sensitivities:gasheartburnheadachenauseadiarrhea

* Please review the disclaimer below.