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  4. NDC Product Code: 69779-003 Emotional Detox

NDC 69779-003 Emotional Detox

Calc Phos,Calc Sulph,Castanea Sativa,Flos,Ilex Aquifolium,Flos,Kali Phos,Nat Mur,Nat - 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
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 69779-003 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:
69779-003
Proprietary Name:
Emotional Detox
Non-Proprietary Name: [1]
Calc Phos, Calc Sulph, Castanea Sativa, Flos, Ilex Aquifolium, Flos, Kali Phos, Nat Mur, Nat Phos, Nat Sulph, Olea Europaea, Flos, Ornithogalum Umbellatum, Flos
Substance Name: [2]
Calcium Sulfate Anhydrous; Castanea Sativa Flower; Ilex Aquifolium Flowering Top; Olea Europaea Flower; Ornithogalum Umbellatum Flowering Top; Potassium Phosphate, Dibasic; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Tribasic Calcium Phosphate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler Name: [5]
Siddha Flower Essences Llc
Labeler Code:
69779
Product Label ID:
385fb878-dd8f-40ae-82a3-874d6a6cceb2
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-09-2015
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
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 a human over the counter drug product labeled by Siddha Flower Essences Llc. The generic name of Emotional Detox is calc phos, calc sulph, castanea sativa, flos, ilex aquifolium, flos, kali phos, nat mur, nat phos, nat sulph, olea europaea, flos, ornithogalum umbellatum, flos. The product's dosage form is spray and is administered via oral form. 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

What are Emotional Detox Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

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:

Which are the Pharmacologic Classes for Emotional Detox?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[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".