NDC 62630-002 Prequimm

Argentum Nitricum, Colchicum Autumnale, Conium Maculatum, Ipecacuanha, Nux Vomica, Pulsatilla (pratensis), Veratrum Album

NDC Product Code 62630-002

NDC CODE: 62630-002

Proprietary Name: Prequimm 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: Argentum Nitricum, Colchicum Autumnale, Conium Maculatum, Ipecacuanha, Nux Vomica, Pulsatilla (pratensis), Veratrum Album 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

NDC 62630-002-17

Package Description: 100 TABLET in 1 BOTTLE

NDC Product Information

Prequimm with NDC 62630-002 is a a human over the counter drug product labeled by Zrg Detox, Inc.. The generic name of Prequimm is argentum nitricum, colchicum autumnale, conium maculatum, ipecacuanha, nux vomica, pulsatilla (pratensis), veratrum album. The product's dosage form is tablet and is administered via oral form.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Prequimm 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.


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.

  • LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
  • MAGNESIUM PALMITOSTEARATE (UNII: R4OXA9G5BV)

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: Zrg Detox, Inc.
Labeler Code: 62630
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: 08-24-2021 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: 12-31-2022 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: N - NO 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".

* Please review the disclaimer below.

Prequimm Product Label Images

Prequimm 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:

Each 300mg tablet contains equal amounts of: Argentum Nitricum 6X, Colchicum Autumnale 4X, 6X, Conium Maculatum 4X, Ipecacuanha 4X, 30X, 200X, Nux Vomica 5X, Pulsatilla (Pratensis)6X, Veratrum Album 8X, 30X, 200X.

Purpose:

Temporarily relieves nausea and vomiting occurring with chemotherapy treatments.

Warnings:

Keep out of reach of children.If pregnant or nursing, ask a healthcare professional before use.Do not use if you have a known allergy to any ingredient in.If symptoms persist or worsen, consult your doctor.In case of overdose, get medical help or contact a Poison Control Center right away.

Keep Out Of Reach Of Children:

Keep out of reach of children.

Directions:

Adults and children over 12 years:dissolve 2 tablets under the tongue every 15 minutes for 2 hours before chemotherapy,then 2 tablets every 4 hours for 7 to 10 days.Children under 12 years: use half the adult dose.

Other Information:

Store tightly closed in a cool and dry place.Tamper evident: Use this product only if neck seal is intact.

Indications:

Temporarily relieves nausea and vomiting occurring with chemotherapy treatments.

Inactive Ingredients:

Lactose, Magnesium Stearate.

Questions:

Distributed by.ZRG Detox, Inc.Calexico, CA 92231www.zrgdetox.com1 (877)737-2583

Package Label Display:

NDC: 62630-002-17PREQUIMMTEMPORARILY RELIEVES NAUSEAAND VOMITING OCCURRING WITHCHEMOTHERAPY TREATMENTSHOMEOPATHIC MEDICINE100TABLETS

* Please review the disclaimer below.