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  4. NDC Product Code: 64578-0084 Kidney-tone

NDC 64578-0084 Kidney-tone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0084?
  4. Kidney-tone 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:
64578-0084
Proprietary Name:
Kidney-tone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Energetix Corp
Labeler Code:
64578
Product Label ID:
82444310-9bfb-45e3-a552-ea072af0f146
Start Marketing Date: [9]
12-05-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 64578-0084?

The NDC code 64578-0084 is assigned by the FDA to the product Kidney-tone which is product labeled by Energetix Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64578-0084-1 59.1 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 Kidney-tone?

Take 30 drops orally twice daily or as directed by a healthcare professional.Consult a physician for use in children under 12 years of age.

Which are Kidney-tone UNII Codes?

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

  • AGRIMONIA EUPATORIA WHOLE (UNII: EBU0U94820)
  • AGRIMONIA EUPATORIA WHOLE (UNII: EBU0U94820) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • CALCIUM OXALATE MONOHYDRATE (UNII: 4PP86KK527)
  • CALCIUM (UNII: SY7Q814VUP) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • LYTTA VESICATORIA (UNII: 3Q034RO3BT)
  • LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
  • EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
  • FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
  • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z)
  • CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z) (Active Moiety)
  • PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
  • PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
  • RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G)
  • RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G) (Active Moiety)
  • SARSAPARILLA (UNII: 2H1576D5WG)
  • SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
  • ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)

Which are Kidney-tone 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".