NDC 84710-101-01 - RoyceDerm Tea Tree Therapeutic
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
- 84710-101
- Requested NDC
- 84710-101-01
- Package NDCs from labels
- 84710-101-01, 84710-101-02
- Manufacturer
- Guangzhou Meixi Pharmaceuticals Co., Ltd.
- Effective date
- 2024-09-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RoyceDerm Tea Tree Therapeutic - Guangzhou Meixi Pharmaceuticals Co., Ltd. | Guangzhou Meixi Pharmaceuticals Co., Ltd. | 2024-09-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84710-101-01 | RoyceDerm Tea Tree Therapeutic | 350 g in 1 BOTTLE | LOTION/SHAMPOO | 350 | 1 | |
| 84710-101-02 | RoyceDerm Tea Tree Therapeutic | 1 in 1 BOX | LOTION/SHAMPOO | 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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| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | ba0868f6-d3de-40e2-bcb3-144fa53062c7 | 2024-12-23 | Warnings | 451W47IQ8X |
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| Rhuli Gel | CAMPHOR, MENTHOL | Trifecta Pharmaceuticals USA, LLC. | 4fbb3c23-ed47-336e-e054-00144ff8d46c | 2024-12-20 | Warnings | L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.