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  4. NDC Product Code: 52731-7020 Pms Complex

NDC 52731-7020 Pms Complex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52731-7020?
  4. Pms Complex Uses
  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:
52731-7020
Proprietary Name:
Pms Complex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nova Homeopathic Therapeutics, Inc.
Labeler Code:
52731
Product Label ID:
6d53dbbe-04d6-40a3-8a2e-64d16f38fdc5
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 52731-7020?

The NDC code 52731-7020 is assigned by the FDA to the product Pms Complex which is product labeled by Nova Homeopathic Therapeutics, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52731-7020-2 1 bottle in 1 box / 50 ml in 1 bottle (52731-7020-1). 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.

What are the uses for Pms Complex?

This product is used as Suggested use for one or more of the following symptoms:Mood swings, mild cramps, bloating, tender breasts, emotional imbalance, lower backache.

Which are Pms Complex UNII Codes?

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

  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • ATROPINE SULFATE (UNII: 03J5ZE7KA5)
  • SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
  • CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • CUPRIC ACETATE (UNII: 39M11XPH03)
  • CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
  • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • TIN (UNII: 387GMG9FH5)
  • TIN (UNII: 387GMG9FH5) (Active Moiety)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)

Which are Pms Complex 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".