NDC 48951-7153 Myristica Argentum
Pellet Oral

Product Information

What is NDC 48951-7153?

The NDC code 48951-7153 is assigned by the FDA to the product Myristica Argentum which is a human over the counter drug product labeled by Uriel Pharmacy Inc. The product's dosage form is pellet and is administered via oral form. The product is distributed in a single package with assigned NDC code 48951-7153-2 1350 pellet in 1 bottle, glass . 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 Code48951-7153
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.
Myristica Argentum
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.
Myristica Argentum
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 FormPellet - 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.
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.
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.
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.
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".
NDC Code Structure

What are the uses for Myristica Argentum?

Product Packages

NDC Code 48951-7153-2

Package Description: 1350 PELLET in 1 BOTTLE, GLASS

Product Details

What are Myristica Argentum 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.
  • POTASSIUM DICHROMATE 6 [hp_X]/1 - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
  • SILVER 20 [hp_X]/1 - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.

* Please review the disclaimer below.

Myristica Argentum 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


Uses: Temporarily relieves symptoms of sinus congestion, sinus headache.

Dosage & Administration

Directions: Dissolve under tongue 4 times daily, up to every hour as needed. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

Otc-Active Ingredient

Active Ingredients: Kalium bichromicum 6X, Tunica mucosa nasi 7X, Argentum nitricum 20X, HPUS.

Inactive Ingredient

Inactive Ingredients: Sucrose,  Myristica sebifera, succus e cort. 4X.

Keep Out Of Reach Of Children


Do Not Use Section

Warnings:  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, 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 Pharmacy

866 642-2858  East Troy, WI 53120 


NDC 48951-7063-2

Principal Display Panel

Myristica Argentum

Sinus Relief

Homeopathic Pellets

net wt. 1 oz.

* Please review the disclaimer below.