Label: CUPRAMINE- cupric sulfate anhydrous liquid
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NDC Code(s):
55999-057-00,
55999-057-01,
55999-057-03,
55999-057-06, view more55999-057-08, 55999-057-09, 55999-057-10, 55999-057-52, 55999-057-54, 55999-057-58, 55999-057-60, 55999-057-62, 55999-057-63
- Packager: Seachem Laboratories Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated August 7, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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VETERINARY INDICATIONS
Copper is the preferred agent for the eradication of Oodinium, Cryptocaryon, Amyloodinium, Ichthyophthirius, and other external parasites in fish.
Cupramine™ is superior to copper sulfate, chloride & citrate: it is non-acidic, less toxic to fish, remains in solution, and does not contaminate the filter bed. It is superior to chelates: it is fully charged (ionic), and active at low concentrations, and is removable with carbon.
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DOSAGE & ADMINISTRATION
DIRECTIONS: Remove all invertebrates. Turn off UV sterilizer; remove chemical filtration. Use 1 mL (top mark of enclosed dispenser) per 40 L (10.5 US gallons) the first day, wait 48 hours, then repeat. In freshwater use half dose. Final copper concentration is 0.5 mg/L (0.25 mg/L in freshwater). Leave at this concentration for 14 days. Do not redose without testing (MultiTest®: Copper). Do not use in conjunction with any other medication. Do not add reducing agents (e.g. dechlorinators, ammonia removers) to water treated with Cupramine™. If tank has ever been treated with an ionic copper (e.g. copper chloride, sulfate or citrate), test copper level after initial dosing. Although most fish tolerate Cupramine™ to 0.8 mg/L, it is not advisable to exceed 0.6 mg/L copper. Remove with carbon or CupriSorb™.
Cu+2 Concentration = 10,000 mg/L
- SAFE HANDLING WARNING
- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 4 L Bottle Label
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INGREDIENTS AND APPEARANCE
CUPRAMINE
cupric sulfate anhydrous liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55999-057 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUPRIC SULFATE ANHYDROUS (UNII: KUW2Q3U1VV) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION 25.1 mg in 1 mL Product Characteristics Color BLUE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55999-057-63 25 in 1 CASE 1 NDC:55999-057-00 50 mL in 1 BOTTLE, PLASTIC 2 NDC:55999-057-60 25 in 1 CASE 2 NDC:55999-057-01 100 mL in 1 BOTTLE, PLASTIC 3 NDC:55999-057-62 25 in 1 CASE 3 NDC:55999-057-03 250 mL in 1 BOTTLE, PLASTIC 4 NDC:55999-057-58 12 in 1 CASE 4 NDC:55999-057-06 500 mL in 1 BOTTLE, PLASTIC 5 NDC:55999-057-54 4 in 1 CASE 5 NDC:55999-057-08 2000 mL in 1 BOTTLE, PLASTIC 6 NDC:55999-057-52 2 in 1 CASE 6 NDC:55999-057-09 4000 mL in 1 BOTTLE, PLASTIC 7 NDC:55999-057-10 20000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 01/01/1980 Labeler - Seachem Laboratories Inc. (133041806) Establishment Name Address ID/FEI Business Operations Seachem Laboratories Inc. 133041806 MANUFACTURE, API MANUFACTURE
