Century 21 Fungal Yeast Infection
NDC 63972-008

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 63972-008?
  4. Century 21 Fungal Yeast Infection 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.

Century 21 Fungal Yeast Infection is a UNAPPROVED HOMEOPATHIC-approved product labeled by 21st Century Homeopathics, Inc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 63972-008 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
63972-008
Proprietary Name:
Century 21 Fungal Yeast Infection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
21st Century Homeopathics, Inc
Labeler Code:
63972
Product Label ID:
983b0a2e-307f-4562-a31a-96b4e1f3e1b8
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-01-1975
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 63972-008?

The NDC code 63972-008 is assigned by the FDA to the product Century 21 Fungal Yeast Infection. This pharmaceutical product is labeled by 21st Century Homeopathics, Inc and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63972-008-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Directions: One (1) teaspoon twice daily or as directed by a healthcare professional.

Which are the associated UNII Codes?

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

  • CANDIDA ALBICANS (UNII: 4D7G21HDBC)
  • CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".