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  4. NDC Product Code: 57520-0502 Hcg Cleanse

NDC 57520-0502 Hcg Cleanse

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57520-0502?
  4. Hcg Cleanse 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:
57520-0502
Proprietary Name:
Hcg Cleanse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca Company
Labeler Code:
57520
Product Label ID:
bbb4462b-ec5e-411c-9e7a-36b02abff420
Start Marketing Date: [9]
08-11-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 57520-0502-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 57520-0502?

The NDC code 57520-0502 is assigned by the FDA to the product Hcg Cleanse which is product labeled by Apotheca Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57520-0502-1 30 ml in 1 bottle, spray . 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 Hcg Cleanse?

INDICATIONS:  Supports weight loss by regulating male and female hormone functions and also suppressing ravenous appetite.

Which are Hcg Cleanse UNII Codes?

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

  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
  • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
  • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
  • BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E)
  • BARIUM CATION (UNII: V645272HLN) (Active Moiety)
  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
  • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
  • SUS SCROFA THYMUS (UNII: 7B69B0BD62)
  • SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
  • SUS SCROFA THYROID (UNII: 6RV024OAUQ)
  • SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB)
  • HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)

Which are Hcg Cleanse 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".