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  4. NDC Product Code: 69779-025 Mind And Memory

NDC 69779-025 Mind And Memory

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69779-025?
  4. Mind And Memory 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:
69779-025
Proprietary Name:
Mind And Memory
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
0d35b9a2-2123-4c14-b0b8-f45f3820ee03
Start Marketing Date: [9]
01-16-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 69779-025?

The NDC code 69779-025 is assigned by the FDA to the product Mind And Memory which is product labeled by Siddha Flower Essences Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69779-025-01 1 bottle in 1 carton / 29.6 ml in 1 bottle. 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 Mind And Memory?

Best if used in the morning and just before beduse 5 days per week until symptoms are relievedadults and children 12 years and over4-5 sprays in mouth twice per daychildren 2 years to under 12 years2-3 sprays in mouth twice per day children under 2 years consult a doctor 

Which are Mind And Memory UNII Codes?

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

Which are Mind And Memory 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".