Rxhomeo Homeopathic Childrens Kit
NDC 15631-2452

View NDC Profile UNII Mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 15631-2452?
  5. Rxhomeo Homeopathic Childrens Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Rxhomeo Homeopathic Childrens Kit is a UNAPPROVED HOMEOPATHIC-approved product labeled by Rxhomeo Private Limited D.b.a.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 15631-2452 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
15631-2452
Proprietary Name:
Rxhomeo Homeopathic Childrens Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Rxhomeo Private Limited D.b.a.
Labeler Code:
15631
Product Label ID:
adc87f76-9674-4759-a767-a5a1a85cb61b
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
06-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I

Product Characteristics

Color(s):
FERRUM PHOSPHORICUM (NDC 15631-0584): WHITE (C48325)
Shape:
FERRUM PHOSPHORICUM (NDC 15631-0584): ROUND (C48348)
Size(s):
FERRUM PHOSPHORICUM (NDC 15631-0584): 3 MM
Score:
FERRUM PHOSPHORICUM (NDC 15631-0584): 1

Code Structure Chart

Product Details

What is NDC 15631-2452?

The NDC code 15631-2452 is assigned by the FDA to the product Rxhomeo Homeopathic Childrens Kit. This pharmaceutical product is labeled by Rxhomeo Private Limited D.b.a. and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 15631-2452-4. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Condition listed above or as directed by the physician

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • ACONITUM NAPELLUS (NDC 15631-0005)
  • ALLIUM CEPA (NDC 15631-0015)
  • ANTIMONIUM TARTARICUM (NDC 15631-0038)
    • ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
    • ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
  • APIS MELLIFICA (NDC 15631-0039)
  • ARSENICUM ALBUM (NDC 15631-0050)
  • ARNICA MONTANA (NDC 15631-0049)
  • BELLADONNA (NDC 15631-0076)
  • BRYONIA ALBA (NDC 15631-0087)
  • CHAMOMILLA (NDC 15631-0123)
  • EUPHRASIA OFFICINALIS (NDC 15631-0184)
  • G SEMPERVIRENS (NDC 15631-0589)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • GLONOINUM (NDC 15631-0207)
  • HYPERICUM PERFORATUM (NDC 15631-0229)
  • IPECACUANHA (NDC 15631-0237)
  • MERCURIUS SOLUBILIS (NDC 15631-0295)
  • NUX VOMICA (NDC 15631-0317)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PODOPHYLLUM PELTATUM (NDC 15631-0354)
  • RHUS TOXICODENDRON (NDC 15631-0374)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • FERRUM PHOSPHORICUM (NDC 15631-0584)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • CALENDULA OFF (NDC 15631-2310)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

  • ACONITUM NAPELLUS (NDC 15631-0005)
  • ALLIUM CEPA (NDC 15631-0015)
  • ANTIMONIUM TARTARICUM (NDC 15631-0038)
  • APIS MELLIFICA (NDC 15631-0039)
  • ARSENICUM ALBUM (NDC 15631-0050)
  • ARNICA MONTANA (NDC 15631-0049)
  • BELLADONNA (NDC 15631-0076)
  • BRYONIA ALBA (NDC 15631-0087)
  • CHAMOMILLA (NDC 15631-0123)
  • EUPHRASIA OFFICINALIS (NDC 15631-0184)
  • G SEMPERVIRENS (NDC 15631-0589)
  • GLONOINUM (NDC 15631-0207)
  • HYPERICUM PERFORATUM (NDC 15631-0229)
  • IPECACUANHA (NDC 15631-0237)
  • MERCURIUS SOLUBILIS (NDC 15631-0295)
  • NUX VOMICA (NDC 15631-0317)
  • PODOPHYLLUM PELTATUM (NDC 15631-0354)
  • RHUS TOXICODENDRON (NDC 15631-0374)
  • FERRUM PHOSPHORICUM (NDC 15631-0584)
  • CALENDULA OFF (NDC 15631-2310)

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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".