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  4. NDC Product Code: 10578-012 Homeopathic Leg Cramp Formula

NDC 10578-012 Homeopathic Leg Cramp Formula

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10578-012?
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10578-012
Proprietary Name:
Homeopathic Leg Cramp Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Indiana Botanic Gardens
Labeler Code:
10578
Product Label ID:
1d11449d-4278-4ba8-96b4-b81ea391b400
Start Marketing Date: [9]
02-01-1998
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
3 MM
Imprint(s):
H;367
Score:
1

Product Packages

NDC Code 10578-012-09

Package Description: 90 TABLET in 1 AMPULE

NDC Code 10578-012-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 10578-012?

The NDC code 10578-012 is assigned by the FDA to the product Homeopathic Leg Cramp Formula which is product labeled by Indiana Botanic Gardens. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10578-012-09 90 tablet in 1 ampule , 10578-012-90 90 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

Which are Homeopathic Leg Cramp Formula UNII Codes?

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

Which are Homeopathic Leg Cramp Formula Inactive Ingredients 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:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".