KANAPLEX- kanamycin a sulfate powder

Kanaplex by

Drug Labeling and Warnings

Kanaplex by is a Animal medication manufactured, distributed, or labeled by Seachem Laboratories Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VETERINARY INDICATIONS

KanaPlex™ is a blended kanamycin based medication that safely and effectively treats several fungal, and bacterial fish diseases (dropsy, popeye, fin/tail rot, septicemia). Because it is absorbed by fish it is useful in treating internal infections in those situations where food is refused. It does not adversely affect the filter bed and is easily removed with carbon.

DOSAGE & ADMINISTRATION

DIRECTIONS: Use 1 level measure (included) to every 20 L (5 gallons). Repeat every 2 days until symptoms disappear or up to a maximum of 3 doses. Turn off UV, ozone, and chemical filtration. To feed, blend 1 measure with about 1 tablespoon of frozen food paste. To minimize loss during feeding use with Focus™. To enhance palatability use with GarlicGuard™ or Entice™. Food may be refrozen.

SPL UNCLASSIFIED SECTION

Active ingredients: kanamycin sulfate (32%)

Inactive ingredients: excipients (68%)

SAFE HANDLING WARNING

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 - 5 g Vial Carton

KanaPlex™

TREATS
FUNGAL &
BACTERIAL
DISEASES

Treats Fungal and Bacterial
Fish Diseases

(Dropsy,Popeye, Fin/Tail Rot,
Septicemia)

Marine & Freshwater

Net Contents: 5 g (0.18 oz)

Seachem®

INGREDIENTS AND APPEARANCE

KANAPLEX 
kanamycin a sulfate powder

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 55999-089
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KANAMYCIN A SULFATE (UNII: J80EX28SMQ) (Kanamycin A - UNII:EQK9Q303C5)	Kanamycin A	317 mg  in 1 g

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55999-089-56	6 in 1 CASE
1	NDC: 55999-089-57	1 in 1 CARTON
1	NDC: 55999-089-12	5 g in 1 VIAL, PLASTIC
2	NDC: 55999-089-15	100 g in 1 VIAL, PLASTIC
3	NDC: 55999-089-18	1000 g in 1 VIAL, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED DRUG OTHER		01/01/1999

Labeler - Seachem Laboratories Inc. (133041806)