Kanaplex: Product Information

KANAPLEX- kanamycin a sulfate powder
Seachem Laboratories Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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.

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.

Active ingredients: kanamycin sulfate (32%)

Inactive ingredients: excipients (68%)

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

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®

PRINCIPAL DISPLAY PANEL -- 5 g Vial Carton
(click image for full-size original)
KANAPLEX
kanamycin a sulfate powder
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55999-089
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
KANAMYCIN A SULFATE (Kanamycin A) Kanamycin A 317 mg in 1 g
Product Characteristics
Color WHITE Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55999-089-56 6 CARTON in 1 CASE contains a CARTON (55999-089-57)
1 NDC:55999-089-57 1 VIAL, PLASTIC in 1 CARTON This package is contained within the CASE (55999-089-56) and contains a VIAL, PLASTIC (55999-089-12)
1 NDC:55999-089-12 5 g in 1 VIAL, PLASTIC This package is contained within a CARTON (55999-089-57) and a CASE (55999-089-56)
2 NDC:55999-089-15 100 g in 1 VIAL, PLASTIC None
3 NDC:55999-089-18 1000 g in 1 VIAL, PLASTIC None
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)

Revised: 07/2018 Seachem Laboratories Inc.

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