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  4. NDC Product Code: 43772-0028 Injury Composition

NDC 43772-0028 Injury Composition

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43772-0028?
  4. Injury Composition 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:
43772-0028
Proprietary Name:
Injury Composition
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Synergy Formulas, Inc.
Labeler Code:
43772
Product Label ID:
ad04c581-290e-462c-979a-f03753d2b9ce
Start Marketing Date: [9]
01-16-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43772-0028?

The NDC code 43772-0028 is assigned by the FDA to the product Injury Composition which is product labeled by Synergy Formulas, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43772-0028-1 60 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 Injury Composition?

For temporary relief of soreness. Pain and swelling in joints. For temporary relief of soreness. Pain and swelling in joints.

Which are Injury Composition UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • ARNICA MONTANA (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • COMFREY ROOT (UNII: M9VVZ08EKQ)
  • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
  • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
  • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)

Which are Injury Composition 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".