NDC 17163-514 - API Super Ick Cure

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
17163-514
Package NDCs from labels
17163-514-02, 17163-514-03, 17163-514-05
Manufacturer
MARS FISHCARE NORTH AMERICA, INC. | Zhejiang Haisen Pharmaceutical Co., Ltd.
Effective date
2026-04-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Drug LabelMARS FISHCARE NORTH AMERICA, INC. | Zhejiang Haisen Pharmaceutical Co., Ltd.2026-04-21OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17163-514-02API Super Ick Cure50 mL in 1 BOTTLE, PLASTICLIQUID507
17163-514-03API Super Ick Cure118 mL in 1 PACKAGELIQUID1187
17163-514-05API Super Ick Cure473 mL in 1 PACKAGELIQUID4737

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17163-514API SUPER ICK CURE (BENZALDEHYDE GREEN) LIQUID [MARS FISHCARE NORTH AMERICA, INC.]53 package rows20240420_baee5c23-c1d4-4d30-9d7f-55e759b5c2ad.zip

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 9 of 9 · 163 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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