SPEC-TUSS- guaifenesin powder

Spec-tuss by

Drug Labeling and Warnings

Spec-tuss by is a Animal medication manufactured, distributed, or labeled by Neogen Corporation-Mercer, Zhejiang Haizhou Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DESCRIPTION

Spec-tuss

Palatable Expectorant Powder

USE IN SPECIFIC POPULATIONS

FOR ANIMAL USE ONLY

Each ounce (28.4 g) contains:
Guaifenesin USP................................2 g (7% w/w)

In a base of sucrose, potassium iodide, ammonium chloride, artificial coloring and flavoring.

Indications:

A palatable powder used as an expectorant in horses.

WARNING:

KEEP OUT OF REACH OF CHILDREN

Warning:

For horses only. Not for human use. Do not use in lactating mares.

Dosage and Administration:

1 teaspoon per 250 lb body weight orally in feed or via dose syringe.

Adult Horses:Not to exceed 1/2 oz twice daily or as directed by your veterinarian.

Foals and Ponies: Consult your veterinarian.

For best results, horse should receive medication for 3-4 days.

STORAGE AND HANDLING

Store in a cool, dry place.

Keep container tightly closed.

SPL UNCLASSIFIED SECTION

Lot No.

Exp. Date:

Manufactured by: Neogen Corporation, Lexington, KY 40511

859-254-1221 • animalsafety.neogen.com   L103-0918

SPL UNCLASSIFIED SECTION

Made in the USA

Item No. 08867

PRINCIPAL DISPLAY PANEL - 1 lb

NDC: 59051-8867-4

Spec-tuss

Palatable Expectorant Powder

NEOGEN® Vet

Net Contents: 1 lb (454 g)

INGREDIENTS AND APPEARANCE

SPEC-TUSS 
guaifenesin powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 59051-8867
Route of Administration	Oral

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	70.4 mg  in 1 g

Product Characteristics
Color		Score
Shape		Size
Flavor	VANILLA	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59051-8867-4	454 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/22/2013

Labeler - Neogen Corporation-Mercer (042125879)

Establishment
Name	Address	ID/FEI	Business Operations
Neogen Corporation-Mercer		042125879	analysis, label, manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Haizhou Pharmaceutical Co., Ltd		530737642	api manufacture