NDC 48951-8300 Silica Skin Support Dks Special Order

Silica Skin Support Dks Special Order

NDC Product Code 48951-8300

NDC CODE: 48951-8300

Proprietary Name: Silica Skin Support Dks Special Order 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: Silica Skin Support Dks Special Order 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.
    • 48951-8300 - Silica Skin Support Dks Special Order

NDC 48951-8300-4

Package Description: 100 g in 1 BOTTLE, GLASS

NDC Product Information

Silica Skin Support Dks Special Order with NDC 48951-8300 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Silica Skin Support Dks Special Order is silica skin support dks special order. The product's dosage form is powder and is administered via oral form.

Labeler Name: Uriel Pharmacy Inc.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

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.

Silica Skin Support Dks Special Order 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.

  • EQUISETUM ARVENSE TOP 5 [hp_X]/g
  • ANTIMONY 5 [hp_X]/g
  • QUERCUS ROBUR WHOLE 9 [hp_X]/g
  • BEEF HEART 9 [hp_X]/g
  • PORK KIDNEY 9 [hp_X]/g
  • MAMMAL LIVER 9 [hp_X]/g
  • BOS TAURUS CARTILAGE 9 [hp_X]/g
  • SUS SCROFA PANCREAS 9 [hp_X]/g
  • SUS SCROFA LUNG 9 [hp_X]/g

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.

  • LACTOSE (UNII: J2B2A4N98G)
  • BEE POLLEN (UNII: 3729L8MA2C)
  • DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
  • ANISE OIL (UNII: 6Y89129C8H)

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 - 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.

Silica Skin Support Dks Special Order Product Label Images

Silica Skin Support Dks Special Order 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

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.

Otc - Active Ingredient

Active Ingredients: Stannum met. (Metallic tin) 3X, Cinis equiseti (Ash of horsetail herb) 5X, Cinis quercus (Decoction of oak bark ash) 9X, Cor (Bovine heart) 9X, Hepar (Bovine liver) 9X, Pancreas (Bovine pancreas) 9X, Pulmo (Bovine lung) 9X, Quercus (Oak) 9X, Renes (Bovine kidneys) 9X, Mesenchyme (Porcine embryonic connective tissue) 11X

Inactive Ingredient

Inactive Ingredients: Lactose, Bee pollen, Diatomaceous earth, Anise oil

Otc - Purpose

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

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: 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.

Otc - Questions

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

* Please review the disclaimer below.