EQUI-SPECTORANT- guaifenesin powder

Equi-Spectorant by

Drug Labeling and Warnings

Equi-Spectorant by is a Animal medication manufactured, distributed, or labeled by MWI/VetOne, Neogen Corporation-Mercer. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​Equi-Spectorant™

​Expectorant 

USE IN SPECIFIC POPULATIONS

​FOR ANIMAL USE ONLY

​Each ounce (28.4g) contains:

Guaifenesin USP..............................2 g (7% w/w)

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

Warnings:

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

FOR VETERINARY USE ONLY

​KEEP OUT OF REACH OF CHILDREN

TAKE TIME

OBSERVE LABEL DIRECTIONS

​Indications:

A palatable powder used as an expectorant in horses. 

Dosage:

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:

​Store in a cool, dry place. Keep container tightly closed.

SPL UNCLASSIFIED SECTION

Lot No.:

Exp. Date:

Distributed by: MWI

Boise, ID 83705

(888) 694-8381

www.VetOne.net

Rev. 09/13

V1 510053

PRINCIPAL DISPLAY PANEL - 1 lb Bottle

NDC: 13985-886-74

Equi-Spectorant™

Expectorant
VETone®
Net Contents: 1 lb (454g)

V1 510053

FOR VETERINARY USE ONLY

KEEP OUT OF REACH OF CHILDREN.

INGREDIENTS AND APPEARANCE

EQUI-SPECTORANT 
guaifenesin powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 13985-886
Route of Administration	Oral

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	70 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)

Product Characteristics
Color		Score
Shape		Size
Flavor	VANILLA	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13985-886-74	454 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/16/2014

Labeler - MWI/VetOne (019926120)

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