NDC 48951-5097 Gelsemium Bryonia
Gelsemium Bryonia
NDC Product Code 48951-5097
Proprietary Name: Gelsemium Bryonia 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: Gelsemium Bryonia 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
- 48951-5097 - Gelsemium Bryonia
NDC 48951-5097-2
Package Description: 1350 PELLET in 1 BOTTLE, GLASS
NDC Product Information
Gelsemium Bryonia with NDC 48951-5097 is a a human over the counter drug product labeled by Uriel Pharmacy Inc. The generic name of Gelsemium Bryonia is gelsemium bryonia. The product's dosage form is pellet and is administered via oral form.
Labeler Name: Uriel Pharmacy Inc
Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
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.
Gelsemium Bryonia 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.
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.
- SUCROSE (UNII: C151H8M554)
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: 12-31-2021 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.
Gelsemium Bryonia Product Label Images
Gelsemium Bryonia 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
- Purpose
- Dosage & Administration
- Otc-Active Ingredient
- Inactive Ingredient
- Keep Out Of Reach Of Children
- Ask Doctor Section
- Pregnancy Or Breast Feeding Section
- Questions Section
Purpose
Uses: Temporarily relieves symptoms of flu, including muscular aches and respiratory symptoms.
Dosage & Administration
Directions: Dissolve under tongue 3-4 times daily. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.
Otc-Active Ingredient
Active Ingredients: Bryonia (White bryony) 3X, Gelsemium (Yellow jasmine) 3X, Vivianite (Nat. ferrous phosphate) 7
Inactive Ingredient
Inactive Ingredient: Sucrose, Vivianite 7X.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Ask Doctor Section
Consult a doctor if symptoms are serious or persist for 3 days, if you are diabetic or intolerant of sugar.
Pregnancy Or Breast Feeding Section
If you are pregnant or nursing, consult a doctor
before use.
Questions Section
Questions? Uriel Pharmacy866 642-2858 East Troy, WI 53120
www.urielpharmacy.comNDC 48951-5005-2
* Please review the disclaimer below.