NDC 57520-0942 Petrochemical Detox

Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Triphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate,

NDC Product Code 57520-0942

NDC Code: 57520-0942

Proprietary Name: Petrochemical Detox What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Triphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, 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.

NDC Code Structure

  • 57520 - Apotheca Company
    • 57520-0942 - Petrochemical Detox

NDC 57520-0942-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Petrochemical Detox with NDC 57520-0942 is a a human over the counter drug product labeled by Apotheca Company. The generic name of Petrochemical Detox is chelidonium majus, symphytum officinale, taraxacum officinale, trifolium pratense, acetone, sodium triphosphate, propylene glycol, sodium benzene sulfonate, ammonium muriaticum, sodium lauryl sulfate,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Apotheca Company

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Petrochemical Detox Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • COMFREY ROOT 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ACETONE 9 [hp_X]/mL
  • SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
  • PROPYLENE GLYCOL 9 [hp_X]/mL
  • BENZENESULFONIC ACID 9 [hp_X]/mL
  • AMMONIUM CHLORIDE 9 [hp_X]/mL
  • SODIUM LAURYL SULFATE 9 [hp_X]/mL
  • TURPENTINE 9 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • CADMIUM SULFIDE 12 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • KEROSENE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PLATINUM 12 [hp_X]/mL
  • LATRODECTUS MACTANS 15 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Apotheca Company
Labeler Code: 57520
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 11-11-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 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.

Exclude Flag: E 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Petrochemical Detox Product Label Images

Petrochemical Detox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Chelidonium majus 3X, Symphytum officinale 3X, Taraxacum officinale 3X, Trifolium pratense 3X, Acetone 9X, 12X, 15X, 30X, Sodium tripolyphosphate 9X, 12X, 15X, 30X, Propylene glycol 9X, 12X, 15X, 30X, Sodium benzene sulfonate 9X, 12X, 15X, 30X, Ammonium muriaticum 9X, 12X, 15X, 30X, Sodium lauryl sulfate 9X, 12X, 15X, 30X, Terebinthina 9X, 12X, 15X, 30X, Arsenicum album 12X, Cadmium sulphuratum 12X, Gelsemium sempervirens 12X, Iridium metallicum 12X, Lycopodium clavatum 12X, Mercurius solubilis 12X, Nitricum acidum 12X, Nux vomica 12X, Petroleum 12X, Phosphoricum acidum 12X, Platinum metallicum 12X, Latrodectus mactans 15X

Otc - Purpose

INDICATIONS:  For temporary relief of symptoms related to petrochemical toxicity including rash, fever, pulmonary inflammation, fatigue, headache, muscle and joint pain, memory/attention disorders, frequent colds, insomnia, and depression.

Warnings

WARNINGS:  Keep out of the reach of children. In case of overdose, contact Physician or Poison Control Center right away. If pregnant or breast-feeding, seek advice of a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Dosage & Administration

DIRECTIONS: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized Water, 25% Ethanol

Otc - Keep Out Of Reach Of Children

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose, contact physician or Poison Control Center right away.

Indications & Usage

INDICATIONS:  For temporary relief of symptoms related to petrochemical toxicity including rash, fever, pulmonary inflammation, fatigue, headache, muscle and joint pain, memory/attention disorders, frequent colds, insomnia, and depression.

Otc - Questions

Dist.By: Deseret Biologicals, Inc.469 Parkland DriveSandy, UT 84070www.desbio.comFor a complete list of Environmental Isode contact Deseret Biologicals, Inc.

* Please review the disclaimer below.

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