NDC 84067-656 - Patch
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
- 84067-656
- Package NDCs from labels
- 84067-656-01
- Manufacturer
- Shantou Youjia E-Commerce Co.,Ltd.
- Effective date
- 2024-05-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Patch - Shantou Youjia E-Commerce Co.,Ltd. | Shantou Youjia E-Commerce Co.,Ltd. | 2024-05-04 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| 179c8fc3-643c-cdb1-e063-6294a90a62ae | 179c8fc3-643b-cdb1-e063-6294a90a62ae | 2024-05-04 | 179c8fc3-643c-cdb1-e063-6294a90a62ae 179c8fc3-643b-cdb1-e063-6294a90a62ae | |||
| AZELEX | AZELAIC ACID | Almirall, LLC | ebdfcaf7-b5d6-47e1-be87-ccaba4b97e75 | 2024-03-04 | Warnings, Adverse reactions | F2VW3D43YT |
| AnubisMed | AZELAIC ACID, SALICYLIC ACID | ANUBIS COSMETICS SL | ebf3153d-30f5-54e4-e053-2995a90a74b1 | 2023-09-05 | Warnings | F2VW3D43YT |
| azelaic acid | AZELAIC ACID | Actavis Pharma, Inc. | 66298d50-d4e2-4852-bbab-581389c488cb | 2022-05-30 | Warnings, Adverse reactions | F2VW3D43YT |
| azelaic acid | AZELAIC ACID | Glenmark Pharmaceuticals Inc., USA | 0b5ab22e-c78a-4429-9a76-a4ba2d11fcde | 2021-12-23 | Warnings, Adverse reactions | F2VW3D43YT |
| Azelaic Acid Gel | AZELAIC ACID | Sandoz Inc. | 66178511-5c1a-4ecd-bc98-2ceb54e710ac | 2021-11-11 | Warnings, Adverse reactions | F2VW3D43YT |
| FINACEA FOAM | AZELAIC ACID | LEO Pharma Inc. | 9fabd24e-4c3b-49a0-aa5f-c8d75ae67572 | 2020-12-08 | Warnings, Adverse reactions | F2VW3D43YT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.