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  4. NDC Product Code: 63083-9234 Myosotis Combination 9234

NDC 63083-9234 Myosotis Combination 9234

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-9234?
  4. Myosotis Combination 9234 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:
63083-9234
Proprietary Name:
Myosotis Combination 9234
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
8cc292dc-b959-4d81-8277-03044992fccb
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63083-9234-1

Package Description: 29.5 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 63083-9234?

The NDC code 63083-9234 is assigned by the FDA to the product Myosotis Combination 9234 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-9234-1 29.5 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 Myosotis Combination 9234?

For the temporary relief of cough, bronchial congestion, minor sore throat, fatigue, or malaise.*

Which are Myosotis Combination 9234 UNII Codes?

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

  • SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T)
  • SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T) (Active Moiety)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G)
  • TEUCRIUM SCORODONIA FLOWERING TOP (UNII: LOK3I16O7G) (Active Moiety)
  • VERONICA BECCABUNGA WHOLE (UNII: 4989JW6TRZ)
  • VERONICA BECCABUNGA WHOLE (UNII: 4989JW6TRZ) (Active Moiety)
  • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25)
  • EQUISETUM HYEMALE WHOLE (UNII: 59677RXH25) (Active Moiety)
  • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
  • FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (Active Moiety)
  • GERANIUM ROBERTIANUM WHOLE (UNII: R5I1HK0UBL)
  • GERANIUM ROBERTIANUM WHOLE (UNII: R5I1HK0UBL) (Active Moiety)
  • MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J)
  • MYOSOTIS ARVENSIS WHOLE (UNII: C73BK97H5J) (Active Moiety)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676)
  • NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS)
  • GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
  • ENGLISH WALNUT (UNII: 1V3SHR7QB7)
  • ENGLISH WALNUT (UNII: 1V3SHR7QB7) (Active Moiety)
  • SMILAX ORNATA ROOT (UNII: 2H1576D5WG)
  • SMILAX ORNATA ROOT (UNII: 2H1576D5WG) (Active Moiety)
  • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5)
  • ARANEUS DIADEMATUS (UNII: 6T6CO7R3Z5) (Active Moiety)
  • ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
  • ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J) (Active Moiety)
  • FERROUS IODIDE (UNII: F5452U54PN)
  • FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
  • BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
  • BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
  • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
  • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)

Which are Myosotis Combination 9234 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".