Pan-zyme-s

Pancreas Balance

Vitality Works, Inc.
Human Otc Drug
NDC 64616-101

Pan-zyme-s also known as Pancreas Balance is a human otc drug labeled by 'Vitality Works, Inc.'. National Drug Code (NDC) number for Pan-zyme-s is 64616-101. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Pan-zyme-s drug includes Arnica Montana Root - 5 [hp_X]/mL Crataegus Fruit - 10 [hp_X]/mL Ether - 10 [hp_X]/mL Lilium Lancifolium Whole Flowering - 10 [hp_X]/mL Manganese Acetate Tetrahydrate - 15 [hp_X]/mL Paraffin - 14 [hp_X]/mL Plantago Major - 10 [hp_X]/mL Sanguinaria Canadensis Root - 10 [hp_X]/mL Silicon Dioxide - 45 [hp_X]/mL Thyroid, Unspecified - 6 [hp_C]/mL and more. The currest status of Pan-zyme-s drug is Active.

Drug Information:

Drug NDC:	64616-101
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:	Pan-zyme-s
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:	Pancreas Balance
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:	ARNICA MONTANA ROOT - 5 [hp_X]/mL CRATAEGUS FRUIT - 10 [hp_X]/mL ETHER - 10 [hp_X]/mL LILIUM LANCIFOLIUM WHOLE FLOWERING - 10 [hp_X]/mL MANGANESE ACETATE TETRAHYDRATE - 15 [hp_X]/mL PARAFFIN - 14 [hp_X]/mL PLANTAGO MAJOR - 10 [hp_X]/mL SANGUINARIA CANADENSIS ROOT - 10 [hp_X]/mL SILICON DIOXIDE - 45 [hp_X]/mL THYROID, UNSPECIFIED - 6 [hp_C]/mL Load more... VALERIAN - 12 [hp_X]/mL WOOD CREOSOTE - 10 [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:	13 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:	MUE8Y11327 Q21UUL2105 0F5N573A2Y X67Z2963PI 9TO51D176N I9O0E3H2ZE W2469WNO6U N9288CD508 ETJ7Z6XBU4 0B4FDL9I6P Load more... JWF5YAW3QW 3JYG22FD73
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.
Pharmacologic Class:	Magnetic Resonance Contrast Activity [MoA] Paramagnetic Contrast Agent [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
64616-101-02	59 mL in 1 BOTTLE, DROPPER (64616-101-02)	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

Pan-zyme-s

Pancreas Balance

Liquid
Vitality Works, Inc.
NDC: 64616-101

Purpose:

Pan-zyme-s gives energy and support to the pancreas to boost functional levels, to increase and balance its enzymatic output, to aid in normalizaion of metabolic and digestive functions

Product Elements:

Pan-zyme-s pancreas balance alcohol water arnica montana root arnica montana root crataegus fruit crataegus fruit ether ether wood creosote wood creosote lilium lancifolium whole flowering lilium lancifolium whole flowering manganese acetate tetrahydrate manganese cation (2+) paraffin paraffin plantago major plantago major sanguinaria canadensis root sanguinaria canadensis root silicon dioxide silicon dioxide thyroid, unspecified thyroid, unspecified valerian valerian

Indications and Usage:

Pan-zyme-s for the temporary relief of digestive sluggishness, flatulence, fatigue and exhaustion.

Warnings:

Pan-zyme-s use only under the direction of a health care professional. do not use if tamper evident seal is broken or missing.

Dosage and Administration:

Pan-zyme-s orally 25 drops, 2 times per day or as indicated by a physician. do not use if tamper evident seal is broken.

Package Label Principal Display Panel:

Pan-zyme-s 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.