PHOS-AID- phosphorus injection

Phos-Aid by

Drug Labeling and Warnings

Phos-Aid by is a Animal medication manufactured, distributed, or labeled by Neogen Corporation, Nova-Tech, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Indications:

For parenteral use as a supplemental source of nutritional phosphorus while the ration is being corrected in areas where feeding rations are inadequate to supply all phosporus needs for cattle.

Each mL contains:

Sodium salt of 4-dimethylamino-2-methylphenyl phosphinic acid 200 mg. Propylene glycol 100 mg. Phenylethanol 6.0 mg. Sodium sulfite 2.0 mg. Water for injection q.s., pH adjusted with sodium carbonate.

Dosage and Administration:

Injectable phosphorous may be administered by intravenous or deep intramuscular injection. Divide high intramuscular dosages between two injection sites. Dosage range is 1 mL per 50 to 100 lbs of body weight. Dose range in cattle is 10 to 20 mL. Two injections are sufficient if the ration deficiency is immediately corrected.

STORAGE AND HANDLING

Store at temperature between 15°-30°C (59° - 86°F).

SPL UNCLASSIFIED SECTION

Manufactured by Nova-Tech

Grand Island, NE 68801 for

Neogen Corporation

Lexington, KY 40511 USA

859/254-1221

L567-92011

Item No. 09070

RMS# 92-303

Made in USA

Net Contents: 100 mL

Lot No.

Exp. Date

Caution:

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

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

PHOS-AID

INGREDIENTS AND APPEARANCE

PHOS-AID 
phosphorus injection

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 59051-9070
Route of Administration	INTRAVENOUS, INTRAMUSCULAR

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLDIMFOS SODIUM (UNII: 6139240O1E) (TOLDIMFOS - UNII:5X1442L8IO)	TOLDIMFOS	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	100 mg  in 1 mL
1-PHENYLETHANOL (UNII: E6O895DQ52)	6 mg  in 1 mL
SODIUM SULFITE (UNII: VTK01UQK3G)	2 mg  in 1 mL
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-9070-5	100 mL in 1 VIAL, MULTI-DOSE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/22/2011

Labeler - Neogen Corporation (042125879)

Registrant - Nova-Tech, Inc (196078976)

Establishment
Name	Address	ID/FEI	Business Operations
Nova-Tech, Inc		196078976	manufacture