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  4. NDC Product Code: 69779-003 Emotional Detox

NDC 69779-003 Emotional Detox

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69779-003?
  4. Emotional Detox 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:
69779-003
Proprietary Name:
Emotional Detox
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
385fb878-dd8f-40ae-82a3-874d6a6cceb2
Start Marketing Date: [9]
04-09-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69779-003?

The NDC code 69779-003 is assigned by the FDA to the product Emotional Detox which is product labeled by Siddha Flower Essences Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69779-003-01 1 bottle in 1 carton / 29.6 ml in 1 bottle, 69779-003-02 1 bottle in 1 carton / 7.5 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 Emotional Detox?

5 sprays in mouth before beduse a maximum of 3 nights per week until symptoms are relievedchildren under 12 years: consult a doctor

Which are Emotional Detox UNII Codes?

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

  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
  • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
  • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
  • POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
  • POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
  • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
  • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)

Which are Emotional Detox 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".