Animal NDC 27135-0353-1 Naturvet Arthrisoothe

Hip And Joint Formula

Animal Product Information

Field Name Field Value
Animal NDC Code 27135-0353-1
Proprietary Name Naturvet Arthrisoothe 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 Hip And Joint Formula 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.
Labeler Name The Garmon Corporation
Product Type Otc Animal Drug
Active Ingredient(s)
  • Alpha-tocopherol Acetate
  • Glucosamine Hydrochloride
  • Yucca Schidigera
  • Omega-3 Fatty Acids
  • Omega-6 Fatty Acids
  • Indian Frankincense
  • Chondroitin Sulfate (bovine)
  • Calcium Ascorbate
  • New Zealand Green Mussel
Inactive Ingredient(s)
  • CITRIC ACID MONOHYDRATE (2968PHW8QP)
  • CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (L11K75P92J)
  • WHEY (8617Z5FMF6)
  • FISH OIL (XGF7L72M0F)
  • FLAX SEED (4110YT348C)
  • MAGNESIUM STEARATE (70097M6I30)
  • MONTMORILLONITE (A585MN1H2L)
  • ROSEMARY (IJ67X351P9)
  • SILICON DIOXIDE (ETJ7Z6XBU4)
  • STEARIC ACID (4ELV7Z65AP)
  • CORN OIL (8470G57WFM)
  • CITRIC ACID MONOHYDRATE (2968PHW8QP)
  • CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (L11K75P92J)
  • WHEY (8617Z5FMF6)
  • FISH OIL (XGF7L72M0F)
  • FLAX SEED (4110YT348C)
  • MAGNESIUM STEARATE (70097M6I30)
  • MONTMORILLONITE (A585MN1H2L)
  • ROSEMARY (IJ67X351P9)
  • SILICON DIOXIDE (ETJ7Z6XBU4)
  • STEARIC ACID (4ELV7Z65AP)
  • CORN OIL (8470G57WFM)
Marketing Category UNAPPROVED DRUG OTHER 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.

Naturvet Arthrisoothe Animal 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.

Table of Contents



Product Facts



Active Ingredients per 500 mg tablet:

Chondroitin Sulfate (Bovine Source)........................................... 116 mg

Glucosamine HCl  (Shellfish Source)............................................ 90 mg

Boswellia Serrata........................................................................ 28 mg

Calcium Ascorbate (from Ester C*)............................................... 22 mg

Yucca Schidigera........................................................................ 17 mg

Green Lipped Mussel (Perna Canaliculus)..................................... 16 mg

dl-Alpha Tocopheryl (Vitamin E)................................................... 29 I.U.

Omega 3 Fatty Acids............................................................... 370 mcg

Omega 6 Fatty Acids............................................................... 700 mcg


Inactive Ingredient



 

Inactive Ingredients:

Citric Acid, Dicalcium Phosphate, Dried Whey, Fish Oil, Flax Seed,

Magnesium Stearate, Montmorillonite Clay, Natural Flavoring, Rosemary

Silical Aerogel, Stearic Acid and Vegetable Oil.


Precautions



Cautions:

Safe use in pregnant animals or animals intended for breeding has

Not been proven.  Consult with your veterinarian before using this

product in animals: with clotting disorders, being treated with

anticoagulant medications, diabetes, or any metabolic disorder

causing hypoglycemia, history of urinary tract stones, or known

allergies to shellfish.  If lameness worsens, discontinue use and

contact your veterinarian.  Administer during or after the

animal has eaten to reduce incidence of gastrointestinal upset.

Federal law prohibits the off-label use of this product in ruminants.


Dosage & Administration



Suggested Use: (Initial Three Week Period)

Weight                                     Amount

Up to 10 lbs.                 2 tablets (1 in AM & 1 in PM)

11 to 39 lbs.                  4 tablets (2 in AM & 2 in PM)

40 to 79 lbs.                  6 tablets (3 in AM & 3 in PM)

80 lbs. and over            9 tablets (4 in AM & 4 in PM)

 

Suggested Use: (Maintenance)

Weight                                     Amount

Up to 10 lbs.                 1 tablet (AM or PM)

11 to 39 lbs.                  2 tablets (1 in AM & 1 in PM)

40 to 79 lbs.                  3 tablets (2 in AM & 1 in PM)

80 lbs. and over            4 tablets (2 in AM & 2 in PM)

 

After the initial three week period, the number of tablets can be reduced

to a level that maintains the pet.  Administration may be increased at any time

depending on the pet's needs.


Warnings



Warnings:

For animal use only.  Kept out of the reach of children and other

Animals.  In case of accidental overdose, contact a health

professional immediately.

 


* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.