NDC 81183-100 The Flower Remedy Peaceful Feeling

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.

Get all the details for National Drug Code (NDC) 81183-100 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
81183-100
Proprietary Name:
The Flower Remedy Peaceful Feeling
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
81183
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-19-2021
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 81183-100?

The NDC code 81183-100 is assigned by the FDA to the product The Flower Remedy Peaceful Feeling which is product labeled by The Flower Remedy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81183-100-30 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 The Flower Remedy Peaceful Feeling?

Use 4 drops under the tongue 4 times daily or as needed

Which are The Flower Remedy Peaceful Feeling UNII Codes?

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

  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
  • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
  • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
  • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU)
  • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU) (Active Moiety)
  • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ)
  • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ) (Active Moiety)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)

Which are The Flower Remedy Peaceful Feeling 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.

[8] 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.

[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, 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".