Greenfish, Body-S

Manufacturer
KOTUKU INC.
Effective date
2016-04-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:45:45

Label at a glance#

ProductGreenfish, Body-S
Active ingredientPOTASSIUM CARBONATE
Label structure1 sections

Label contents#

Full prescribing information#

Greenfish, Body-S

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

body sbody s

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70610-102-012020-01-31C16284748780-19d75b9cf-f3fe-f424-e053-dadaa90a57ceGreenfish, Body-S

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70610-102-01Greenfish, Body-S80 mL in 1 BOTTLE, SPRAYLIQUID805

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70610-102GREENFISH, BODY-S (POTASSIUM CARBONATE) LIQUID [KOTUKU INC.]5Legacy NDC, 1 package rows20160419_e1358e79-d493-4213-9405-61b678552e37.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70610-10270610-102-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
810ec626-d2d7-4acd-a80e-168a9bbc44e1e1358e79-d493-4213-9405-61b678552e372016-04-18WarningsExact identifier
spl id: 810ec626-d2d7-4acd-a80e-168a9bbc44e1
spl set id: e1358e79-d493-4213-9405-61b678552e37

Reported adverse events (FAERS/openFDA)#

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