NDC 48951-2118 Berberis Oxalis
Liquid Oral

Product Information

What is NDC 48951-2118?

The NDC code 48951-2118 is assigned by the FDA to the product Berberis Oxalis which is a human over the counter drug product labeled by Uriel Pharmacy Inc.. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 48951-2118-1 10 ampule in 1 box / 1 ml in 1 ampule. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code48951-2118
Proprietary Name 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.		Berberis Oxalis
Non-Proprietary Name 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.		Berberis Oxalis
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.		Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.		Uriel Pharmacy Inc.
Labeler Code48951
Marketing Category 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.		UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		09-01-2009
Listing Expiration Date 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.		12-31-2023
Exclude Flag 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I". 		N
NDC Code Structure

What are the uses for Berberis Oxalis?


Product Packages

NDC Code 48951-2118-1

Package Description: 10 AMPULE in 1 BOX / 1 mL in 1 AMPULE

Product Details

What are Berberis Oxalis Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Berberis Oxalis Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Indications & Usage



Directions: FOR ORAL USE ONLY.


Dosage & Administration



Take the contents of one ampule
under the tongue and hold for
30 seconds, then swallow.


Otc - Active Ingredient



Active Ingredients: Berberis e pl. tota
2X, Oxalis e pl. tota 3X, Sabal serr. e
fruct. 3X, Urtica urens ex herba 3X,
Viscum Abietis e pl. tota 4X, Magnesium
sulf. 6X, Prostata 8X, Granite 10X


Inactive Ingredient



Inactive Ingredients: Water, Salt


Otc - Purpose



Use: Temporary relief of headache.


Otc - Keep Out Of Reach Of Children



KEEP OUT OF REACH OF CHILDREN.


Warnings



Warnings: Do not use if allergic to any ingredient. Consult a doctor before use
for serious conditions or if conditions
worsen or persist. If pregnant or nursing, consult a doctor before use. Natural ingredients may cause color, scent
and/or taste variation.


Otc - Questions



Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com


Package Label.Principal Display Panel




* Please review the disclaimer below.