NDC 70558-0002 Detox

Beta Vulgaris, Boldo, Chelidonium Majus, Sarsaparilla (smilax Regelii), Gelsemium Sempervirens, Veratrum Album, Ferrum Metallicum, Iodium, Lycopodium Clavatum, Nux Vomica, Pulsatilla (vulgaris), Selenium Metallicum, Thuja Occidentalis, Zincum Metallicum

NDC Product Code 70558-0002

NDC Code: 70558-0002

Proprietary Name: 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: Beta Vulgaris, Boldo, Chelidonium Majus, Sarsaparilla (smilax Regelii), Gelsemium Sempervirens, Veratrum Album, Ferrum Metallicum, Iodium, Lycopodium Clavatum, Nux Vomica, Pulsatilla (vulgaris), Selenium Metallicum, Thuja Occidentalis, Zincum Metallicum 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.


Code Structure
  • 70558 - Pro Weight Loss Inc.
    • 70558-0002 - Detox

NDC 70558-0002-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Detox with NDC 70558-0002 is a a human over the counter drug product labeled by Pro Weight Loss Inc.. The generic name of Detox is beta vulgaris, boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (vulgaris), selenium metallicum, thuja occidentalis, zincum metallicum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Pro Weight Loss Inc.

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.


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.

  • BETA VULGARIS 3 [hp_X]/mL
  • PEUMUS BOLDUS LEAF 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • SMILAX ORNATA ROOT 6 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 7 [hp_X]/mL
  • VERATRUM ALBUM ROOT 7 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PULSATILLA VULGARIS 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
  • ZINC 12 [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: Pro Weight Loss Inc.
Labeler Code: 70558
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: 04-14-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 06-27-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N 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.

Detox Product Label Images

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

Active Ingredients:

Beta Vulgaris 3X, Boldo 3X, Chelidonium Majus 3X, Sarsaparilla (Smilax Regelii) 6X, Gelsemium Sempervirens 7X, Veratrum Album 7X, Ferrum Metallicum 12X, Iodium 12X, Lycopodium Clavatum 12X, Nux Vomica 12X, Pulsatilla (Vulgaris) 12X, Selenium Metallicum 12X, Thuja Occidentalis 12X, Zincum Metallicum 12X.

Homeopathic Indications:

For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

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

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

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

Inactive Ingredients:

Demineralized water, 25% ethanol

Questions:

Distributed byPro Weight Loss, 94 Boylston Cir.Shrewsbury, MA 01545 • 508-842-4600

Package Label Display:

NDC 70558-0002-1Pro Weight LossThe Fat Burning ScienceHOMEOPATHICDetox1 FL OZ (30 ml)

* Please review the disclaimer below.

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