Equi-Spectorant

Manufacturer: MWI/VetOne | Neogen Corporation-Mercer
Effective date: 2020-05-02
Label type: OTC ANIMAL DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 23:32:58

Label at a glance#

ProductEqui-Spectorant

Active ingredientGUAIFENESIN

Label structure10 sections

Storage and handling

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

Contacts and useful links#

PhoneLabel contact859-254-1221

PhoneLabel contact800-621-8829

PhoneLabel contact(888) 694-8381

Websitewww.vetone.net

www.VetOne.net

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Equi-Spectorant

Powder

Expectorant

USE IN SPECIFIC POPULATIONS SECTION

For veterinary use only

Each ounce (28.4g) contains:

COMPONENTS

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

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

Warnings:

WARNINGS AND PRECAUTIONS SECTION

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

Indications:

INDICATIONS & USAGE SECTION

A palatable powder used as an expectorant in horses.

Dosage:

DOSAGE & ADMINISTRATION SECTION

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:

STORAGE AND HANDLING SECTION

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

OTC - QUESTIONS SECTION

Questions? Call 859-254-1221 or toll-free at 800-621-8829.

SPL UNCLASSIFIED SECTION

Lot No.:

Exp. Date:

Distributed by: MWI

Boise, ID 83705

(888) 694-8381

www.VetOne.net

Rev. 10/19

PRINCIPAL DISPLAY PANEL - 1 lb Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 13985-886-74

VETone®

Equi-Spectorant

Powder

Expectorant

For veterinary use only.

Keep out of reach of children.

Net Contents: 1 lb (454g)

V1 510053

Equi-Spectorant 1lb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	2
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	2
AMMONIUM CHLORIDE	INACTIVE INGREDIENT	01Q9PC255D	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Equi-Spectorant
Guaifenesin
AMMONIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
13985-886	13985-886-74

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMMONIUM CHLORIDE	01Q9PC255D	IACT
GUAIFENESIN	495W7451VQ	ACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
AMMONIUM CHLORIDE	AMMONIUM CHLORIDE	01Q9PC255D	TABLET / ORAL		8 mg	Exact identifier — unii candidate 5 equally ranked IID candidates
AMMONIUM CHLORIDE	AMMONIUM CHLORIDE	01Q9PC255D	TABLET, FILM COATED / ORAL	8 mg		Exact identifier — unii candidate 5 equally ranked IID candidates
AMMONIUM CHLORIDE	AMMONIUM CHLORIDE	01Q9PC255D	SYRUP / ORAL	131.68 mg/5ml		Exact identifier — unii candidate 5 equally ranked IID candidates
AMMONIUM CHLORIDE	AMMONIUM CHLORIDE	01Q9PC255D	TABLET, EXTENDED RELEASE / ORAL		21 mg	Exact identifier — unii candidate 5 equally ranked IID candidates
AMMONIUM CHLORIDE	AMMONIUM CHLORIDE	01Q9PC255D	CAPSULE / ORAL		8 mg	Exact identifier — unii candidate 5 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Join
Ammonium muriaticum	AMMONIUM CHLORIDE	Boiron	687eae27-d686-1a0f-e053-2a91aa0a124a	2023-10-16	Name fallback generic name: AMMONIUM CHLORIDE
Ammonium muriaticum	AMMONIUM CHLORIDE	Boiron	84b58da5-40e4-f3c1-e053-2991aa0aeb82	2023-08-29	Name fallback generic name: AMMONIUM CHLORIDE
Ammonium muriaticum	AMMONIUM CHLORIDE	Boiron	8427af63-5644-be0c-e053-2a91aa0a255d	2023-05-16	Name fallback generic name: AMMONIUM CHLORIDE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.