NDC 63083-7009 Ret Heart 7009

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-7009
Proprietary Name:
Ret Heart 7009
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
63083
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 63083-7009?

The NDC code 63083-7009 is assigned by the FDA to the product Ret Heart 7009 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-7009-1 29.5 ml in 1 bottle, dropper . 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 Ret Heart 7009?

Temporarily relieves indifference, intolerance, impatience, irritation, overenthusiasm, hyperactivity, dread, sadness, or anxiousness.*

Which are Ret Heart 7009 UNII Codes?

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

  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
  • VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ)
  • VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ) (Active Moiety)
  • POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
  • POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
  • GOLD (UNII: 79Y1949PYO)
  • GOLD (UNII: 79Y1949PYO) (Active Moiety)
  • CAUSTICUM (UNII: DD5FO1WKFU)
  • CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
  • SAFFRON (UNII: E849G4X5YJ)
  • SAFFRON (UNII: E849G4X5YJ) (Active Moiety)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)

Which are Ret Heart 7009 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:

* Please review the disclaimer below.

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".