NDC 83071-020-01 - Dr.Jucre Rebirth Activating Toner
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
- 83071-020
- Requested NDC
- 83071-020-01
- Package NDCs from labels
- 83071-020-01, 83071-020-02
- Manufacturer
- NATURECELL CO., LTD. | Cosmax, Inc.
- Effective date
- 2022-11-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dr.Jucre Rebirth Activating Toner - NATURECELL CO., LTD. | Cosmax, Inc. | NATURECELL CO., LTD. | Cosmax, Inc. | 2022-11-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83071-020-01 | Dr.Jucre Rebirth Activating Toner | 150 mL in 1 BOTTLE | LIQUID | 150 | 1 | |
| 83071-020-02 | Dr.Jucre Rebirth Activating Toner | 1 in 1 CARTON | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.