Silica Comp.

Uriel Pharmacy Inc.
Human Otc Drug
NDC 48951-8327

Silica Comp. is a human otc drug labeled by 'Uriel Pharmacy Inc.'. National Drug Code (NDC) number for Silica Comp. is 48951-8327. This drug is available in dosage form of Powder. The names of the active, medicinal ingredients in Silica Comp. drug includes Beef Heart - 9 [hp_X]/g Bos Taurus Cartilage - 11 [hp_X]/g Equisetum Arvense Top - 5 [hp_X]/g Mammal Liver - 9 [hp_X]/g Pork Kidney - 9 [hp_X]/g Quercus Robur Whole - 9 [hp_X]/g Sus Scrofa Lung - 9 [hp_X]/g Sus Scrofa Pancreas - 9 [hp_X]/g . The currest status of Silica Comp. drug is Active.

Drug Information:

Drug NDC:	48951-8327
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Silica Comp.
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Silica Comp.
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Uriel Pharmacy Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Powder
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	BEEF HEART - 9 [hp_X]/g BOS TAURUS CARTILAGE - 11 [hp_X]/g EQUISETUM ARVENSE TOP - 5 [hp_X]/g MAMMAL LIVER - 9 [hp_X]/g PORK KIDNEY - 9 [hp_X]/g QUERCUS ROBUR WHOLE - 9 [hp_X]/g SUS SCROFA LUNG - 9 [hp_X]/g SUS SCROFA PANCREAS - 9 [hp_X]/g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	01 Sep, 2009
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	09 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Uriel Pharmacy Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UNII:	P47W069U38 UE77B10IIY 1DP6Y6B65Z X7BCI5P86H R7QMG0BT2W 7GL3G1COB3 9Y3J3362RY
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
48951-8327-4	100 g in 1 BOTTLE, GLASS (48951-8327-4)	01 Sep, 2009	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Silica Comp.

Powder
Uriel Pharmacy Inc.
NDC: 48951-8327

Purpose:

Uses: to promote skin elasticity and strengthen hair and nails.

Product Elements:

Silica comp. silica comp. equisetum arvense top equisetum arvense top quercus robur whole quercus robur whole beef heart beef heart bee pollen diatomaceous earth mammal liver mammal liver sus scrofa pancreas sus scrofa pancreas sus scrofa lung sus scrofa lung pork kidney pork kidney bos taurus cartilage bos taurus cartilage lactose, unspecified form anhydrous lactose anise oil

Indications and Usage:

Directions: for oral use only.

Warnings:

Warnings: claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated. do not use if allergic to any ingredient. contains lactose. 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.

Dosage and Administration:

Take regularly before meals with a small amount of water. ages 12 and older: 1 teaspoon. ages 2-11: 1/2 teaspoon. under age 2: consult a doctor.

Package Label Principal Display Panel:

Silica comp powder

Further Questions:

Questions? call 866.642.2858 made with care by uriel, east troy, wi 53120 www.shopuriel.com lot:

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.