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#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70610-102-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-f3fe-f424-e053-dadaa90a57ce | Greenfish, Body-S |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70610-102-01 | Greenfish, Body-S | 80 mL in 1 BOTTLE, SPRAY | LIQUID | 80 | 5 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Greenfish, Body-S
- POTASSIUM CARBONATE
- CARBONATE ION
- CITRIC ACID MONOHYDRATE
- CALCIUM HYDROXIDE
- HYPROMELLOSES
- water
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70610-102 | 70610-102-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM CARBONATE | BQN1B9B9HA | ACTIB |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| CALCIUM HYDROXIDE | PF5DZW74VN | IACT |
| HYPROMELLOSES | 3NXW29V3WO | IACT |
| water | 059QF0KO0R | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 810ec626-d2d7-4acd-a80e-168a9bbc44e1 | e1358e79-d493-4213-9405-61b678552e37 | 2016-04-18 | Warnings | 810ec626-d2d7-4acd-a80e-168a9bbc44e1 e1358e79-d493-4213-9405-61b678552e37 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
