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  4. NDC Product Code: 52731-7035 Lymphatic Complex

NDC 52731-7035 Lymphatic Complex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52731-7035?
  4. Lymphatic 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:
52731-7035
Proprietary Name:
Lymphatic 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:
10e0a7a1-22f0-4a56-8c29-011bf66f447c
Start Marketing Date: [9]
06-01-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52731-7035-2

Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (52731-7035-1)

Product Details

What is NDC 52731-7035?

The NDC code 52731-7035 is assigned by the FDA to the product Lymphatic 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 52731-7035-2 1 bottle in 1 box / 50 ml in 1 bottle (52731-7035-1). 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 Lymphatic Complex?

This product is used as Suggested use for one or more of the following symptoms:Inflammation,swollen lymph nodes, low immune system, effects of toxins.

Which are Lymphatic Complex UNII Codes?

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

  • BARIUM CARBONATE (UNII: 6P669D8HQ8)
  • BARIUM CATION (UNII: V645272HLN) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
  • CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • GALIUM APARINE (UNII: Z4B6561488)
  • GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
  • GRAPHITE (UNII: 4QQN74LH4O)
  • GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
  • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K)
  • JUGLANS REGIA FRUIT RIND, IMMATURE (UNII: ZPS7Q5U53K) (Active Moiety)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • URTICA URENS (UNII: IHN2NQ5OF9)
  • URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)

Which are Lymphatic 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".