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  4. NDC Product Code: 55924-1001 Advantage

NDC 55924-1001 Advantage

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55924-1001?
  4. Advantage 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:
55924-1001
Proprietary Name:
Advantage
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Soza Clinic
Labeler Code:
55924
Product Label ID:
be0d6578-88b9-4dc9-a669-25299800dd8d
Start Marketing Date: [9]
12-15-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 55924-1001?

The NDC code 55924-1001 is assigned by the FDA to the product Advantage which is product labeled by Soza Clinic. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55924-1001-1 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 Advantage?

Temporarily relieves symptoms of:  hunger cravings, overeating, excessive appetite, cravings for sweets & starches. Temporarily relieves symptoms of: hunger cravings, overeating, excessive appetite, cravings for sweets & starches.

Which are Advantage 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)
  • BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E)
  • BARIUM CATION (UNII: V645272HLN) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • FUCUS VESICULOSUS (UNII: 535G2ABX9M)
  • FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
  • GRAPHITE (UNII: 4QQN74LH4O)
  • GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
  • SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
  • SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (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)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • SUS SCROFA THYROID (UNII: 6RV024OAUQ)
  • SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
  • THYMUS SERPYLLUM (UNII: 86H4S6K51N)
  • THYMUS SERPYLLUM (UNII: 86H4S6K51N) (Active Moiety)

Which are Advantage 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".