VITAMIN AD- retinol cholecalciferol injection

VITAMIN AD by

Drug Labeling and Warnings

VITAMIN AD by is a Animal medication manufactured, distributed, or labeled by Phoenix Pharmaceutical Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

INDICATIONS

For use as a supplemental nutritive source of vitamins A and D in cattle, sheep and swine.

CAUTION

Do not inject into meat animals within 60 days of marketing. 

Administration of this product to well nourished animals may cause hypervitaminosis D which may result in hypercalcemia.  This condition may be harmful to the animal.

DOSAGE AND ADMINISTRATION

Inject intramuscularly or subcutaneously preferably  in the neck area using aseptic technique.

Calves - 1/2 to 1 mL

Adult Cattle - 2 to 4 mL

Lambs - 1/4 to 1/2 mL

Adult Sheep - 1 to 2 mL

Weaning Pigs - 1/4 to 1/2 mL

Adult Swine - 1 to 2 mL

These suggested dosage may be repeated after 60 days, if necessary.

TAKE TIME OBSERVE LABEL DIRECTIONS

COMPOSITION

Each mL of sterile solution contains:
Vitamin A  . . . . . . . . . 500,000 IU
Vitamin D3  . . . . . . . . . 75,000 IU
In an emulsifiable base with vitamin E (antioxidant), N-methylpyrrolidone, polyoxyethylated (30) castor oil, propylene glycol dicaprylate, polyoxyethylene (20) sorbitan monooleate and benzyl alcohol 2%.

STORAGE

Store at controlled room temperature between 15o and 30oC (59-86oF).

Protect from light and excessive heat.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VITAMIN AD 
retinol cholecalciferol injection

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 57319-424
Route of Administration	INTRAMUSCULAR, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91)	RETINOL	500000 [iU]  in 1 mL
CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41)	CHOLECALCIFEROL	75000 [iU]  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57319-424-06	250 mL in 1 VIAL
2	NDC: 57319-424-06	250 mL in 1 VIAL

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/15/2004

Labeler - Phoenix Pharmaceutical Inc (150711039)