FDA.reportPublic FDA data

Sulfaplex

Manufacturer
Seachem Laboratories Inc.
Effective date
2018-07-16
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:40:17

Label at a glance#

ProductSulfaplex
Active ingredientSulfathiazole
Label structure7 sections

Label contents#

Full prescribing information#

VETERINARY INDICATIONS SECTION

SulfaPlex™ is an effective and safe treatment for many bacterial, fungal and protozoan infestations in the aquarium. It is easily removed with carbon and does not impair nitrification.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Use 2 to 3 measures (included, each about 100 mg) to every 40 L (10 US gallons).This dose may be increased up to four-fold if symptoms do not subside. Repeat every 3 days for up to 3 weeks or until symptoms disappear. Do not use UV, ozone, or chemical filtration during use.

SPL UNCLASSIFIED SECTION

Active ingredients: sulfathiazole (69%).

SPL UNCLASSIFIED SECTION

Inactive ingredients: excipients (31%)

SAFE HANDLING WARNING SECTION

For use in ornamental aquariums only. Not for human consumption.

SPL UNCLASSIFIED SECTION

Seachem Laboratories Inc. • 1000 Seachem Drive, Madison, GA 30650

www.seachem.com • support@seachem.com

PRINCIPAL DISPLAY PANEL - 10 g Vial Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SulfaPlex™

BACTERIAL
FUNGAL &
PROTOZOAN
INFESTATIONS

Treats Many Bacterial, Fungal
and Protozoan Infestations

Marine & Freshwater

Net Contents: 10 g (0.35 oz)

Seachem®

PRINCIPAL DISPLAY PANEL - 10 g Vial Carton
PRINCIPAL DISPLAY PANEL - 10 g Vial Carton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55999-085-13Sulfaplex10 g in 1 VIAL, PLASTICPOWDER101
55999-085-15Sulfaplex100 g in 1 VIAL, PLASTICPOWDER1001
55999-085-20Sulfaplex4000 g in 1 VIAL, PLASTICPOWDER40001
55999-085-56Sulfaplex6 in 1 CASEPOWDER61
55999-085-57Sulfaplex1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55999-085SULFAPLEX (SULFATHIAZOLE) POWDER [SEACHEM LABORATORIES INC.]15 package rows20180723_638cfdf4-99cc-4c33-9144-ebadf96a9512.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55999-08555999-085-13, 55999-085-57, 55999-085-56, 55999-085-15, 55999-085-20

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SulfathiazoleY7FKS2XWQHACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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