NDC 59779-858 Gallbladder Relief

Belladonna, Carduus Marianus, Chelidonium Majus, Colocynthis, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vornica, Phosphorus, Pulsatilla, Veratrum Album

NDC Product Code 59779-858

NDC Code: 59779-858

Proprietary Name: Gallbladder 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: Belladonna, Carduus Marianus, Chelidonium Majus, Colocynthis, Lycopodium Clavatum, Natrum Sulphuricum, Nux Vornica, Phosphorus, Pulsatilla, Veratrum Album 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

  • 59779 - Woonsocket Prescr Ctr Inc
    • 59779-858 - Gallbladder Relief

NDC 59779-858-00

Package Description: 60 TABLET in 1 BOTTLE

NDC Product Information

Gallbladder Relief with NDC 59779-858 is a a human over the counter drug product labeled by Woonsocket Prescr Ctr Inc. The generic name of Gallbladder Relief is belladonna, carduus marianus, chelidonium majus, colocynthis, lycopodium clavatum, natrum sulphuricum, nux vornica, phosphorus, pulsatilla, veratrum album. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Woonsocket Prescr Ctr Inc

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Gallbladder 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.

  • ATROPA BELLADONNA 30 [hp_X]/601
  • MILK THISTLE 30 [hp_X]/601
  • CHELIDONIUM MAJUS 30 [hp_X]/601
  • CITRULLUS COLOCYNTHIS FRUIT PULP 30 [hp_X]/601
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/601
  • SODIUM SULFATE 30 [hp_X]/601
  • STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/601
  • PHOSPHORUS 30 [hp_X]/601
  • PULSATILLA VULGARIS 30 [hp_X]/601
  • VERATRUM ALBUM ROOT 30 [hp_X]/601

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.

  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • MANNITOL (UNII: 3OWL53L36A)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

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: Woonsocket Prescr Ctr Inc
Labeler Code: 59779
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: 11-11-2014 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: 12-31-2019 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.

Gallbladder Relief Product Label Images

Gallbladder 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

Active Ingredients                                        PurposesBelladonna 30X ......................................... Inflated colonCarduus Marianus 30X ................................... GallstonesChelidonium Majus 30X .................................. GallstonesColocynthis 30X .............................................. CrampingLycopodium Clavatum 30X ................... Sour EructationsNatrum Sulphuricum 30X ............................... DyspepsiaNux Vomica 30X ............................................ GallstonesPhosphorus 30X ................................................ GastritisPulsatilla 30X ........................................... Epigastric PainVeratrum Album 30X .................................. Constipation

Otc - Purpose

UsesFor temporary relief of constipation, belching, and abdominal discomfort due to the gallbladder.

Otc - 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.

Indications & Usage

  • CVSNEW!Homeopathic GALLBLADDER RELIEFFAST & EFFECTIVETemporary relief of: ConstipationBelchingAbdominal discomfort60 Quick Dissolving TabletsHomeopathic Medicine

Dosage & Administration

DirectionsAdults & children 12 times and over: Dissolve one tablet under tongue, three times daily or as otherwise directed by a health professional.Children under 12: Consult a doctor prior to use.

Warnings

WarningsDo not use if you have ever had an allergic reaction to this product or any of its ingredients.Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.If pregnant or breast-feeding, ask a doctor before using product.

Inactive Ingredient

Inactive IngredientsAdvantol® 300, lactose, magnesium stearate, mannitol, microcrystalline cellulose.

* Please review the disclaimer below.

Previous Code
59779-857
Next Code
59779-860