Muskel

Anti-interleukin-1.alpha. Immunoglobulin G Rabbit, Bos Taurus Ankle Joint, Sus Scrofa Ankle Joint, Bos Taurus Joint Capsule, Sus Scrofa Joint Capsule, Brain-derived Neurotrophic Factor Human, Metenkefalin, Ersofermin, Bos Taurus Solar Plexus, Sus Scrofa Solar Plexus, Calcitonin, Bos Taurus Frontal Lobe, Sus Scrofa Frontal Lobe, Bos Taurus Hip Joint, Sus Scrofa Hip Joint, Bos Taurus Hippocampus, Sus Scrofa Hippocampus, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Mecasermin Rinfabate


Viatrexx Bio Incorporated
Human Otc Drug
NDC 63776-347
Muskel also known as Anti-interleukin-1.alpha. Immunoglobulin G Rabbit, Bos Taurus Ankle Joint, Sus Scrofa Ankle Joint, Bos Taurus Joint Capsule, Sus Scrofa Joint Capsule, Brain-derived Neurotrophic Factor Human, Metenkefalin, Ersofermin, Bos Taurus Solar Plexus, Sus Scrofa Solar Plexus, Calcitonin, Bos Taurus Frontal Lobe, Sus Scrofa Frontal Lobe, Bos Taurus Hip Joint, Sus Scrofa Hip Joint, Bos Taurus Hippocampus, Sus Scrofa Hippocampus, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Mecasermin Rinfabate is a human otc drug labeled by 'Viatrexx Bio Incorporated'. National Drug Code (NDC) number for Muskel is 63776-347. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Muskel drug includes Anti-interleukin-1.alpha. Immunoglobulin G Rabbit - 200 [kp_C]/mL Beef - 200 [kp_C]/mL Bos Taurus Ankle Joint - 200 [kp_C]/mL Bos Taurus Frontal Lobe - 200 [kp_C]/mL Bos Taurus Hip Joint - 200 [kp_C]/mL Bos Taurus Hippocampus - 200 [kp_C]/mL Bos Taurus Hypothalamus - 200 [kp_C]/mL Bos Taurus Joint Capsule - 200 [kp_C]/mL Bos Taurus Nerve - 200 [kp_C]/mL Bos Taurus Solar Plexus - 200 [kp_C]/mL and more. The currest status of Muskel drug is Active.

Drug Information:

Drug NDC: 63776-347
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: Muskel
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: Anti-interleukin-1.alpha. Immunoglobulin G Rabbit, Bos Taurus Ankle Joint, Sus Scrofa Ankle Joint, Bos Taurus Joint Capsule, Sus Scrofa Joint Capsule, Brain-derived Neurotrophic Factor Human, Metenkefalin, Ersofermin, Bos Taurus Solar Plexus, Sus Scrofa Solar Plexus, Calcitonin, Bos Taurus Frontal Lobe, Sus Scrofa Frontal Lobe, Bos Taurus Hip Joint, Sus Scrofa Hip Joint, Bos Taurus Hippocampus, Sus Scrofa Hippocampus, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Mecasermin Rinfabate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Viatrexx Bio Incorporated
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Spray
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:ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT - 200 [kp_C]/mL
BEEF - 200 [kp_C]/mL
BOS TAURUS ANKLE JOINT - 200 [kp_C]/mL
BOS TAURUS FRONTAL LOBE - 200 [kp_C]/mL
BOS TAURUS HIP JOINT - 200 [kp_C]/mL
BOS TAURUS HIPPOCAMPUS - 200 [kp_C]/mL
BOS TAURUS HYPOTHALAMUS - 200 [kp_C]/mL
BOS TAURUS JOINT CAPSULE - 200 [kp_C]/mL
BOS TAURUS NERVE - 200 [kp_C]/mL
BOS TAURUS SOLAR PLEXUS - 200 [kp_C]/mL
BOS TAURUS SPINAL CORD - 200 [kp_C]/mL
BOS TAURUS SYMPATHETIC NERVE - 200 [kp_C]/mL
BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN - 200 [kp_C]/mL
CALCITONIN - 200 [kp_C]/mL
ERSOFERMIN - 200 [kp_C]/mL
INTERLEUKIN-10 - 200 [kp_C]/mL
MECASERMIN RINFABATE - 200 [kp_C]/mL
METENKEFALIN - 200 [kp_C]/mL
PORK - 200 [kp_C]/mL
SUS SCROFA ANKLE JOINT - 200 [kp_C]/mL
SUS SCROFA FRONTAL LOBE - 200 [kp_C]/mL
SUS SCROFA HIP JOINT - 200 [kp_C]/mL
SUS SCROFA HIPPOCAMPUS - 200 [kp_C]/mL
SUS SCROFA HYPOTHALAMUS - 200 [kp_C]/mL
SUS SCROFA JOINT CAPSULE - 200 [kp_C]/mL
SUS SCROFA NERVE - 200 [kp_C]/mL
SUS SCROFA SOLAR PLEXUS - 200 [kp_C]/mL
SUS SCROFA SPINAL CORD - 200 [kp_C]/mL
SUS SCROFA SYMPATHETIC NERVE - 200 [kp_C]/mL
TRANSFORMING GROWTH FACTOR BETA-1 - 200 [kp_C]/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: 26 Mar, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 08 May, 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:VIATREXX BIO INCORPORATED
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.
UPC:0063776347151
UPC stands for Universal Product Code.
NUI:N0000185371
N0000175629
N0000184306
M0000728
M0006342
N0000185017
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:ML4QRZ1HCL
4PIB2155QP
63Z8OTG0HU
R8970AT87X
Y8426REN4E
4UQ8473K2W
S6G2NLH4Y7
782I3O9VSM
28G2U3MQJK
Y8H8S1X8IB
03Z3I85RNE
WU6MQV435F
A1ED6W905I
DF35I47HCM
1NWT5SW3NW
9SC4O216V9
NZ8M50KKRG
9JEZ9OD3AS
O138UB266J
654134QUOV
GV54Q19G55
519062UA90
5U2M8VE56F
N6R0856Z79
LX0XHE5NLN
JXV50I6ZHK
WN6M3MGG1X
AVM99FC8AI
H6L0IFR3FE
T7D25J14LT
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 EPC:Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:Allergens [CS]
Dietary Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Allergens [CS]
Cell-mediated Immunity [PE]
Dietary Proteins [CS]
Increased Histamine Release [PE]
Meat Proteins [EXT]
Non-Standardized Food Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63776-347-151 BOTTLE, SPRAY in 1 BOX (63776-347-15) / 50 mL in 1 BOTTLE, SPRAY26 Mar, 2012N/ANo
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.

Purpose:

Purpose anti-interleukin-1 anti-inflammation ankle articulation regeneration articular capsule regeneration brain derived neurotrophic factor regeneration beta endorphin pain relief bfibroblast growth factor regeneration coelliac plexus regeneration calcitonin calcium balance frontal lobe regeneration hip articulation regeneration hippocampus regeneration hypothalamus regeneration insulin-like growth factor regeneration interleukin-10 anti-inflammation muscle regeneration nerve regeneration spinal cord regeneration sympathetic trunk regeneration transforming growth factor-beta regeneration

Product Elements:

Muskel anti-interleukin-1.alpha. immunoglobulin g rabbit, bos taurus ankle joint, sus scrofa ankle joint, bos taurus joint capsule, sus scrofa joint capsule, brain-derived neurotrophic factor human, metenkefalin, ersofermin, bos taurus solar plexus, sus scrofa solar plexus, calcitonin, bos taurus frontal lobe, sus scrofa frontal lobe, bos taurus hip joint, sus scrofa hip joint, bos taurus hippocampus, sus scrofa hippocampus, bos taurus hypothalamus, sus scrofa hypothalamus, mecasermin rinfabate sus scrofa hip joint sus scrofa hip joint bos taurus hippocampus bos taurus hippocampus sus scrofa hippocampus sus scrofa hippocampus bos taurus hypothalamus bos taurus hypothalamus sus scrofa hypothalamus sus scrofa hypothalamus mecasermin rinfabate mecasermin interleukin-10 interleukin-10 beef beef pork pork bos taurus nerve bos taurus nerve sus scrofa nerve sus scrofa nerve bos taurus spinal cord bos taurus spinal cord sus scrofa spinal cord sus scrofa spinal cord bos taurus sympathetic nerve bos taurus sympathetic nerve sus scrofa sympathetic nerve sus scrofa sympathetic nerve transforming growth factor beta-1 transforming growth factor beta-1 alcohol water anti-interleukin-1.alpha. immunoglobulin g rabbit anti-interleukin-1.alpha. immunoglobulin g rabbit bos taurus ankle joint bos taurus ankle joint sus scrofa ankle joint sus scrofa ankle joint bos taurus joint capsule bos taurus joint capsule sus scrofa joint capsule sus scrofa joint capsule brain-derived neurotrophic factor human brain-derived neurotrophic factor human metenkefalin metenkefalin ersofermin ersofermin bos taurus solar plexus bos taurus solar plexus sus scrofa solar plexus sus scrofa solar plexus calcitonin calcitonin bos taurus frontal lobe bos taurus frontal lobe sus scrofa frontal lobe sus scrofa frontal lobe bos taurus hip joint bos taurus hip joint

Indications and Usage:

Uses to help assist with muscle, nerve and skeletal repair & regeneration

Warnings:

Warnings stop use and ask a health care practitioner if symptoms persist for more than five days or worsen. if pregnant or breastfeeding, ask a health care practitioner before use.

Dosage and Administration:

Dosage 1-5 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Package Label Principal Display Panel:

Principal display panel item: vpc0420 ndc 63776-347-15 homeopathic remedy muskel • to help assist with muscle, nerve and skeletal repair & regeneration oral spray 50ml 1.7 oz viatrexx ™ bio incorporated manufactured by viatrexx www.viatrexx.com newark, de 19713 muskel 50 ml 1.7 oz viatrexx ™ bio incorporated item: vpc0420 ndc: 63776-347-15 indications: to help assist with muscle, nerve and skeletal repair & regeneration directions: 1-5 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner. mfg. for viatrexx bio inccorporated. www.viatrexx.com newark, de 19713 carton label

Further Questions:

Questions info@viatrexx.com


Comments/ Reviews:

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