NDC 48951-6011 Kali Phos. Aurum
Kali Phos. Aurum
NDC Product Code 48951-6011
Proprietary Name: Kali Phos. Aurum 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: Kali Phos. Aurum 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.
- 48951-6011 - Kali Phos. Aurum
NDC 48951-6011-4
Package Description: 250 TABLET in 1 BOTTLE, GLASS
NDC Product Information
Kali Phos. Aurum with NDC 48951-6011 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Kali Phos. Aurum is kali phos. aurum. The product's dosage form is tablet and is administered via oral form.
Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
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.
Kali Phos. Aurum 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.
- FERROUS SULFATE 5 [hp_X]/1
- GOLD 10 [hp_X]/1
- POTASSIUM PHOSPHATE, MONOBASIC 6 [hp_X]/1
- SILICON DIOXIDE 5 [hp_X]/1
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)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
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.
Pharmacological Class(es)
What is a Pharmacological Class?These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
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.
Kali Phos. Aurum Product Label Images
Kali Phos. Aurum 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
- Dosage & Administration
- Otc - Active Ingredient
- Inactive Ingredient
- Otc - Purpose
- Otc - Keep Out Of Reach Of Children
- Warnings
- Otc - Questions
Indications & Usage
Directions: FOR ORAL USE ONLY.
Dosage & Administration
Take 3-4 times daily. Ages 12 and older: 1-2 tablets. Ages 2-11: 1 tablet. Under age 2: Consult a doctor.
Otc - Active Ingredient
Active Ingredients: 100gm contains: 3.3gm Kali phosphoricum 6X, 3.3gm Aurum met. 10X, 2gm Ferrum sulf. 5X, 0.8gm Quartz 5X
Inactive Ingredient
Inactive Ingredients: Lactose, Stearic acid, Magnesium stearate
Otc - Purpose
Uses: Temporary relief of nervousness and exhaustion.
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 Uriel, East Troy, WI 53120 www.urielpharmacy.com
* Please review the disclaimer below.