NDC 63776-100 Connectissue

Anti-interleukin-1.alpha. Immunoglobulin G Rabbit, Ascorbic Acid, Metenkefalin, Ersofermin, Bos Taurus Cartilage, Sus Scrofa Cartilage, Pork Collagen, Bos Taurus Red Blood Cell, Sus Scrofa Red Blood Cell, Interleukin-3, Interleukin-3, Beef Liver, Pork Liver, Beef, Pork, Bos Taurus Tendon, Sus Scrofa Tendon, Cetermin

NDC Product Code 63776-100

NDC 63776-100-14

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Connectissue with NDC 63776-100 is a a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Connectissue is anti-interleukin-1.alpha. immunoglobulin g rabbit, ascorbic acid, metenkefalin, ersofermin, bos taurus cartilage, sus scrofa cartilage, pork collagen, bos taurus red blood cell, sus scrofa red blood cell, interleukin-3, interleukin-3, beef liver, pork liver, beef, pork, bos taurus tendon, sus scrofa tendon, cetermin. The product's dosage form is spray and is administered via oral form.

Labeler Name: Viatrexx Bio Incorporated

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Connectissue 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.

  • ASCORBIC ACID 30 [kp_C]/mL
  • METENKEFALIN 200 [kp_C]/mL
  • ERSOFERMIN 200 [kp_C]/mL
  • PORK COLLAGEN 200 [kp_C]/mL
  • INTERLEUKIN-3 200 [kp_C]/mL
  • BEEF LIVER 200 [kp_C]/mL
  • PORK LIVER 200 [kp_C]/mL
  • BEEF 200 [kp_C]/mL
  • PORK 200 [kp_C]/mL
  • BOS TAURUS TENDON 200 [kp_C]/mL
  • SUS SCROFA TENDON 200 [kp_C]/mL
  • CETERMIN 200 [kp_C]/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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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.
  • 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: Viatrexx Bio Incorporated
Labeler Code: 63776
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: 03-26-2012 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: 12-31-2020 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 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.

Connectissue 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

Anti-Interleukin-1 9 9X 200K, Ascorbic acid 8X 30K, Beta endorphin 8 9X 200K, bFibroblast Growth Factor 8 9X 200K, Cartilage 6X 200K, Collagen 8X 200K, Erythrocytes 8X 200K, Interleukin 3 3 12X 200K, Liver 6X 200K, Muscle 6X 200K, Tendon 8X 200K, Transforming Growth Factor-2 11X 200K


Anti-Interleukin-1Anti-inflammationAscorbic acidAnti-oxidantBeta endorphinPain reliefbFibroblast Growth FactorRegenerationCartilageRegenerationCollagenRegenerationErythrocytesImmune supportInterleukin 3Immune supportLiver RegenerationMuscleRegenerationTendonRegenerationTransforming Growth Factor-2Immune support


To help support the repair & regeneration of connective tissue & cartilage.


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.


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

Other Ingredients

Alcohol and Water

Other Information

Normal storage use.Do not use if tamper-evident seal is broken or removed.

* Please review the disclaimer below.