NDC 73510-526-01 - LingLongJiuHuo Linglong Moxibustion Wormwood Moxibustion 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
- 73510-526
- Requested NDC
- 73510-526-01
- Package NDCs from labels
- 73510-526-01, 73510-526-11, 73510-526-20
- Manufacturer
- Shanghai Jingqin Biological Technology Co., Ltd. | Hubei Lishizhen Modern Biological Medicine Group Co.,Ltd.
- Effective date
- 2022-10-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| LingLongJiuHuo Linglong Moxibustion Wormwood Moxibustion Patch | Shanghai Jingqin Biological Technology Co., Ltd. | Hubei Lishizhen Modern Biological Medicine Group Co.,Ltd. | 2022-10-15 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73510-526-20 | 2024-01-30 | C162847 | 48780-1 | 1030e365-40f0-111a-e063-dadaa90a10e2 | LingLongJiuHuo Linglong Moxibustion, JingQin |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73510-526-01 | LingLongJiuHuo Linglong Moxibustion Wormwood Moxibustion Patch | 1 g in 1 PACKET | TAPE | 1 | 1 | |
| 73510-526-11 | LingLongJiuHuo Linglong Moxibustion Wormwood Moxibustion Patch | 10 in 1 BAG | TAPE | 10 | 1 | |
| 73510-526-20 | LingLongJiuHuo Linglong Moxibustion Wormwood Moxibustion Patch | 1 in 1 BOX | TAPE | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 73510-526 | LINGLONGJIUHUO LINGLONG MOXIBUSTION WORMWOOD MOXIBUSTION PATCH (HERBAL MOXIBUSTION) TAPE [SHANGHAI JINGQIN BIOLOGICAL TECHNOLOGY CO., LTD.] | 1 | Legacy NDC, 3 package rows | 20221018_eae50138-0c0c-65a0-e053-2995a90af13d.zip |
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 |
|---|---|---|---|---|---|---|
| Eyewash | EYEWASH | Global Equipment Company | c4f78121-4668-2e0c-e053-2995a90ab6c6 | 2021-06-17 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Asclemed USA, Inc. | 45c38269-883c-4198-a9d5-03810a4420ec | 2021-01-14 | Warnings, Adverse reactions | 059QF0KO0R |
| Bach Original Flower Remedies | WATER | Nelson Bach USA Limited | 09c76050-42c5-4403-865c-a1f6f668d9c0 | 2020-06-15 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 8bcf5572-49e1-4302-9522-56f57904cb4a | 2019-12-29 | Warnings, Adverse reactions | 059QF0KO0R |
| Dynamic Eyewash with Eyecup | WATER | Dynamic Safety International | 7d3af0f4-0e1f-9ea5-e053-2991aa0af7a2 | 2018-12-17 | Warnings | 059QF0KO0R |
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| 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.