NDC 48951-3083 Chicory Ginger Digestive Bitters

Silybum Marianum Seed Gentiana Lutea Root Artemisia Vulgaris Root Ginger Chelidonium Majus Black Pepper

NDC Product Code 48951-3083

NDC Code: 48951-3083

Proprietary Name: Chicory Ginger Digestive Bitters 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: Silybum Marianum Seed Gentiana Lutea Root Artemisia Vulgaris Root Ginger Chelidonium Majus Black Pepper 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

  • 48951 - Uriel Pharmacy Inc
    • 48951-3083 - Chicory Ginger Digestive Bitters

NDC 48951-3083-3

Package Description: 1200 LIQUID in 1 BOTTLE, DROPPER

NDC 48951-3083-9

Package Description: 5200 LIQUID in 1 BOTTLE, GLASS

NDC Product Information

Chicory Ginger Digestive Bitters with NDC 48951-3083 is a a human over the counter drug product labeled by Uriel Pharmacy Inc. The generic name of Chicory Ginger Digestive Bitters is silybum marianum seed gentiana lutea root artemisia vulgaris root ginger chelidonium majus black pepper. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Uriel Pharmacy 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.

Chicory Ginger Digestive Bitters 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.

  • GINGER 1 [hp_X]/1
  • BLACK PEPPER 3 [hp_X]/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.

  • 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: Uriel Pharmacy Inc
Labeler Code: 48951
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: 09-01-2009 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.

Chicory Ginger Digestive Bitters Product Label Images

Chicory Ginger Digestive Bitters 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


Uses: Improves digestion; eases gas, nausea and indigestion.

Dosage & Administration

Directions: Take by mouth diluted with water or undiluted. Before meals: Ages 12 and older: 1/4 teaspoon. Ages 2-11: 1/8 teaspoon. For nausea or indigestion: Ages 12 and older: 1/2 teaspoon. Ages 2-11: 1/4 teaspoon. Under age 2: Ask a doctor. SHAKE WELL BEFORE USE. Refrigerate after opening.

Otc-Active Ingredient

Active Ingredients: Carduus marianus e fruct. 1X, Gentiana e rad. 1X, Artemesia vulgaris ex herba 1X, Zingiberis e rhiz. 1X, Chelidonium e rad. 3X, Piper nigrum e fruct. 3X, all HPUS.

Inactive Ingredient

Inactive Ingredients: Water, Cichorium e rad., Calamus e rhiz., Curcuma e rhiz., Lime oil.

Keep Out Of Reach Of Children


Do Not Use Section

Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask Doctor Section

Consult a doctor if symptoms persist or worsen.

Pregnancy Or Breast Feeding Section

If you are pregnant or nursing, consult a doctor
before use.

Questions Section

Made with care byUriel PharmacyEast Troy, WI 53120Questions or comments?Please call 1.866.642.2858www.urielpharmacy.com

* Please review the disclaimer below.

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