VITAMIN AD- retinol cholecalciferol injection

Vitamin AD by

Drug Labeling and Warnings

Vitamin AD by is a Animal medication manufactured, distributed, or labeled by Durvet, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

For Animal Use Only

KEEP OUT OF REACH OF CHILDREN

INJECTABLE STERILE SOLUTION

Restricted Drug (CA) - Use Only as Directed

INDICATIONS

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

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,
Yearling Cattle-1 to 2 mL
Adult Cattle- 2 to 4 mL,

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

COMPONENTS

Each mL of sterile solution contains:

ACTIVE INGREDIENTS

Vitamin A  . . . . . . . . . 500,000 IU
Vitamin D3  . . . . . . . . . 75,000 IU

INACTIVE INGREDIENTS

Emulsifiable base with vitamin E (antioxidant), N-methylpyrrolidone, polyoxyethylated (30) castor oil, propylene glycol dicaprylate, polyoxyethylene (20) sorbitan monooleate and benzyl alcohol 2%.

STORAGE AND HANDLING

Store at controlled room temperature between 15° and 30°C (59°-86°F)

Protect from light and excessive heat.

TAKE TIME OBSERVE LABEL DIRECTIONS

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VITAMIN AD 
retinol cholecalciferol injection

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-327
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: 30798-327-10	100 mL in 1 VIAL
2	NDC: 30798-327-13	250 mL in 1 VIAL
3	NDC: 30798-327-17	500 mL in 1 VIAL

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/25/2000

Labeler - Durvet, Inc. (056387798)