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  4. NDC Product Code: 50114-4426 Body Pure

NDC 50114-4426 Body Pure

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50114-4426?
  5. Body Pure Uses
  6. Active Ingredients UNII Codes
  7. 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:
50114-4426
Proprietary Name:
Body Pure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Heel Inc
Labeler Code:
50114
Product Label ID:
85fb5a1a-e0c6-4dc2-b3de-4cc0f6afa490
Start Marketing Date: [9]
08-30-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
BHI;O;M
Score:
1

Code Structure Chart

Product Details

What is NDC 50114-4426?

The NDC code 50114-4426 is assigned by the FDA to the product Body Pure which is product labeled by Heel Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50114-4426-2 100 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.

What are the uses for Body Pure?

For the temporary relief of:FatigueMild Skin RashesNausea and Headaches

Which are Body Pure UNII Codes?

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

  • .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
  • .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y) (Active Moiety)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
  • RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX)
  • RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • VIOLA TRICOLOR (UNII: 9Q24RAI43V)
  • VIOLA TRICOLOR (UNII: 9Q24RAI43V) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • CAFFEINE (UNII: 3G6A5W338E)
  • CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
  • FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F)
  • FRANGULA PURSHIANA BARK (UNII: 4VBP01X99F) (Active Moiety)
  • URTICA URENS (UNII: IHN2NQ5OF9)
  • URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
  • CHOLESTEROL (UNII: 97C5T2UQ7J)
  • CHOLESTEROL (UNII: 97C5T2UQ7J) (Active Moiety)
  • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED) (UNII: WC4E824FQ9)
  • INFLUENZA A VIRUS A/SINGAPORE/6/86 (H1N1) ANTIGEN (HEAT INACTIVATED) (UNII: WC4E824FQ9) (Active Moiety)
  • KEROSENE (UNII: 1C89KKC04E)
  • KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
  • TOBACCO LEAF (UNII: 6YR2608RSU)
  • TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P)
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)

Which are Body Pure 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".