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  4. NDC Product Code: 69779-015 Youthful Skin

NDC 69779-015 Youthful Skin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69779-015?
  4. Youthful Skin 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:
69779-015
Proprietary Name:
Youthful Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
6f72f1b9-d627-4110-9546-13320e62c465
Start Marketing Date: [9]
04-09-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 69779-015?

The NDC code 69779-015 is assigned by the FDA to the product Youthful Skin 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 69779-015-01 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 Youthful Skin?

4-5 sprays and gently massage into desired area twice per dayfor minor skin irritation use 5 or more times per dayuse 5 days per week until symptoms are relievedchildren under 2 years: consult a doctor

Which are Youthful Skin UNII Codes?

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

Which are Youthful Skin 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".