warnings
WARNINGS For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Refrain from using it on wounded areas. Keep out of reach of children.
Dr.Jucre Rebirth
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Dr.Jucre Rebirth
- Generic name
- NIACINAMIDE
- Manufacturer
- NATURECELL CO., LTD.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2ab4562d-e8b4-c9a4-e063-6394a90ada47
- SPL ID
- 2ab4562d-e8b5-c9a4-e063-6394a90ada47
- Version
- 1
- Effective date
- 2025-01-02
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:25:19
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Dr.Jucre Rebirth | openfda.brand_name | |
| generic name | NIACINAMIDE | openfda.generic_name | |
| manufacturer name | NATURECELL CO., LTD. | openfda.manufacturer_name | |
| ndc | package | 83071-140-01 | openfda.package_ndc |
| ndc | package | 83071-140-02 | openfda.package_ndc |
| ndc | product | 83071-140 | openfda.product_ndc |
| ndc11 | package | 83071014002 | derived:openfda.package_ndc |
| ndc11 | package | 83071014001 | derived:openfda.package_ndc |
| spl id | 2ab4562d-e8b5-c9a4-e063-6394a90ada47 | id | |
| spl set id | 2ab4562d-e8b4-c9a4-e063-6394a90ada47 | set_id | |
| unii | 25X51I8RD4 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.