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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|---|---|---|---|---|---|---|
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| Oimmal Gentle Eye Wash | SODIUM CHLORIDE | Shenzhen Shandian Jingling Technology Co., Ltd. | 4bb4e59b-a43e-fa38-e063-6294a90aea71 | 2026-02-26 | Warnings | 451W47IQ8X |
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| Potassium Citrate and Citric Acid | POTASSIUM CITRATE AND CITRIC ACID | Chartwell Governmental & Specialty RX, LLC. | fd57a176-7faf-4053-b348-6ba5f192f05a | 2026-02-25 | Warnings, Adverse reactions | 2968PHW8QP |
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| Advanced Pain Relief Roll-On Gel With 5% Natural Menthol | MENTHOL | Allure Labs | 4bad597f-acb2-a122-e063-6394a90a9fcf | 2026-02-25 | Warnings | L7T10EIP3A |
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| Antiseptic Rinse Spring Mint | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Family Dollar Stores, Inc | 974e97c5-a255-4bb4-9ec9-5edc3f7899eb | 2026-02-24 | Warnings, Adverse reactions | L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.