NDC 72630-030-01 - DR.PLINUS ZERO TROUBLE
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
- 72630-030
- Requested NDC
- 72630-030-01
- Package NDCs from labels
- 72630-030-01, 72630-030-02
- Manufacturer
- S Skin Co., Ltd. | BIOCOSONE CO.,LTD
- Effective date
- 2022-10-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DR.PLINUS ZERO TROUBLE - S Skin Co., Ltd. | BIOCOSONE CO.,LTD | S Skin Co., Ltd. | BIOCOSONE CO.,LTD | 2022-10-18 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72630-030-02 | 2022-10-14 | C162847 | 48780-1 | e4f33bdf-9b87-d8a0-e053-dadaa90a6e4e | ca117510-27f2-4344-8241-fdb564de1901 |
| 72630-030-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-9b87-d8a0-e053-dadaa90a6e4e | ca117510-27f2-4344-8241-fdb564de1901 |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.