Sweep

Detoxifying

Vitality Works, Inc.
Human Otc Drug
NDC 64616-105

Sweep also known as Detoxifying is a human otc drug labeled by 'Vitality Works, Inc.'. National Drug Code (NDC) number for Sweep is 64616-105. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Sweep drug includes Activated Charcoal - 10 [hp_X]/mL Ammi Visnaga Fruit - 10 [hp_X]/mL Carbo Animalis - 20 [hp_X]/mL Citrullus Colocynthis Fruit Pulp - 7 [hp_X]/mL Daphne Mezereum Bark - 10 [hp_X]/mL Nitric Acid - 20 [hp_X]/mL Palladium - 14 [hp_X]/mL Platinum - 15 [hp_X]/mL Potassium Arsenite Anhydrous - 20 [hp_X]/mL Quinine Arsenate - 14 [hp_X]/mL and more. The currest status of Sweep drug is Active.

Drug Information:

Drug NDC:	64616-105
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Sweep
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Detoxifying
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Vitality Works, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACTIVATED CHARCOAL - 10 [hp_X]/mL AMMI VISNAGA FRUIT - 10 [hp_X]/mL CARBO ANIMALIS - 20 [hp_X]/mL CITRULLUS COLOCYNTHIS FRUIT PULP - 7 [hp_X]/mL DAPHNE MEZEREUM BARK - 10 [hp_X]/mL NITRIC ACID - 20 [hp_X]/mL PALLADIUM - 14 [hp_X]/mL PLATINUM - 15 [hp_X]/mL POTASSIUM ARSENITE ANHYDROUS - 20 [hp_X]/mL QUININE ARSENATE - 14 [hp_X]/mL Load more... SARSAPARILLA - 15 [hp_X]/mL SELENIUM - 20 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	08 Apr, 2013
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	25 Jun, 2026
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Vitality Works, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UNII:	2P3VWU3H10 3UN285QN0C 279O8I0433 23H32AOH17 X2N6E405GV 411VRN1TV4 5TWQ1V240M 49DFR088MY BM2U42PAKI 8C15XFK30P Load more... 2H1576D5WG H6241UJ22B
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
64616-105-02	59 mL in 1 BOTTLE, DROPPER (64616-105-02)	08 Apr, 2013	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Sweep

Detoxifying

Liquid
Vitality Works, Inc.
NDC: 64616-105

Purpose:

Sweep helps in the detoxification of the body

Product Elements:

Sweep detoxifying alcohol water ammi visnaga fruit ammi visnaga fruit carbo animalis carbo animalis activated charcoal activated charcoal quinine arsenate arsenate ion citrullus colocynthis fruit pulp citrullus colocynthis fruit pulp potassium arsenite anhydrous arsenite ion daphne mezereum bark daphne mezereum bark nitric acid nitric acid palladium palladium platinum platinum sarsaparilla sarsaparilla selenium selenium

Indications and Usage:

Sweep for the temprory relief of bloating, tiredness, nausea and vertigo.

Warnings:

Sweep use only under the drection of a health care professional. do not use if tamper evident seal is broken or missing.

Dosage and Administration:

Sweep orally 25 drops, 2 times per day or as indicated by a physician. children 12 and under use one half the adult dosage.

Package Label Principal Display Panel:

Sweep label

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.