Label: CANINE WITH EPIITALIS FOR JOINT AND CARTILAGE MATRIX SUPPORT- - granule
- NDC Code(s): 76208-001-53, 76208-001-56, 76208-001-62
- Packager: American Aquatic Testing, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 11, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- DESCRIPTION
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
-
WARNINGS AND PRECAUTIONS
Cautions:
Safe use in pregnant animals or animals intended for breeding has not been proven.
Do not use in animals with known allergies to shellfish.
If lameness worsens, discontinue use and contact your veterinarian.
An examination from a veterinarian is recommended prior to using this product.
Warnings:
Keep out of the reach of children and animals. In case of
accidental overdose, contact a
health professional immediately
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CANINE WITH EPIITALIS FOR JOINT AND CARTILAGE MATRIX SUPPORT
- granuleProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:76208-001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEW ZEALAND GREEN MUSSEL (UNII: 1L5332YQ7U) (NEW ZEALAND GREEN MUSSEL - UNII:1L5332YQ7U) NEW ZEALAND GREEN MUSSEL 408 mg in 1 g BLACKFOOT ABALONE (UNII: 1KU16741MK) (BLACKFOOT ABALONE - UNII:1KU16741MK) BLACKFOOT ABALONE 136 mg in 1 g SHARK (UNII: KEK41AP35U) (SHARK - UNII:KEK41AP35U) SHARK 136 mg in 1 g PLATYCLADUS ORIENTALIS SEED (UNII: QDB7SF78HO) (PLATYCLADUS ORIENTALIS SEED - UNII:QDB7SF78HO) PLATYCLADUS ORIENTALIS SEED 54 mg in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76208-001-53 100 g in 1 BOTTLE 2 NDC:76208-001-56 10 g in 1 POUCH 3 NDC:76208-001-62 50 g in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/11/2011 Labeler - American Aquatic Testing, Inc. (847862299) Registrant - Interpath Pty. Ltd. (744466777) Establishment Name Address ID/FEI Business Operations Nutrizeal Limited 590627915 manufacture Establishment Name Address ID/FEI Business Operations Cawthron Institute 590501698 analysis
