NDC 48951-2055 Berberis Quartz

Berberis Quartz

  1. Labeler Index
  2. Uriel Pharmacy Inc.
  3. NDC: 48951-2055 Berberis Quartz

NDC Product Code 48951-2055

NDC CODE: 48951-2055

Proprietary Name: Berberis Quartz 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: Berberis Quartz 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.

Product Characteristics

Color(s):
WHITE (C48325)
Shape: ROUND (C48348)
Size(s):
3 MM
Score: 1

NDC Code Structure

  • 48951 - Uriel Pharmacy Inc.

NDC 48951-2055-2

Package Description: 1350 PELLET in 1 BOTTLE, GLASS

NDC Product Information

Berberis Quartz with NDC 48951-2055 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Berberis Quartz is berberis quartz. The product's dosage form is pellet and is administered via oral form.

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.

Berberis Quartz 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: 12-31-2022 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 - NO 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".

* Please review the disclaimer below.

Berberis Quartz Product Label Images

Berberis Quartz 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

Indications & Usage

Directions: FOR ORAL USE ONLY.

Dosage & Administration

Dissolve pellets under the tongue 3-4


times daily. Ages 12 and older: 10 pellets.


Ages 2-11: 5 pellets. Under age 2: Consult


a doctor.

Otc - Active Ingredient

Active Ingredients: Berberis (Barberry) 3X, Tunica mucosa nasi (Bovine nasal mucosa) 7X, Quartz (Rock crystal) 20X

Inactive Ingredient

Inactive Ingredient: Sucrose

Otc - Purpose

Use: Temporary relief of sinus congestion.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Do not use if safety seal is broken or missing. Natural ingredients may cause color, scent and/or taste variation.

Otc - Questions

Questions? Call 866.642.2858


Uriel, East Troy WI 53120

* Please review the disclaimer below.