NDC 44911-0633 Vaccistat

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44911-0633
Proprietary Name:
Vaccistat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
44911
Start Marketing Date: [9]
01-04-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 44911-0633?

The NDC code 44911-0633 is assigned by the FDA to the product Vaccistat which is product labeled by Energique, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44911-0633-1 30 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 Vaccistat?

May temporarily relieve skin irritation, dry cough, eczema, and fever.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve skin irritation, dry cough, eczema, and fever.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Which are Vaccistat UNII Codes?

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

  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • ALUMINUM OXIDE (UNII: LMI26O6933) (Active Moiety)
  • ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
  • ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
  • DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
  • DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
  • MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • VACCINIA VIRUS (UNII: JDS6958QAG)
  • VACCINIA VIRUS (UNII: JDS6958QAG) (Active Moiety)
  • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK)
  • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (Active Moiety)

Which are Vaccistat 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:

* Please review the disclaimer below.

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".