NDC 84008-003-01 - Pain Relief Gel-Tube
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
- 84008-003
- Requested NDC
- 84008-003-01
- Package NDCs from labels
- 84008-003-01, 84008-003-02
- Manufacturer
- Bullet point LLC | ShanghaiChuangshiMedicalTechnology(Group)Co.,Ltd.
- Effective date
- 2025-11-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pain Relief Gel-Tube | Bullet point LLC | ShanghaiChuangshiMedicalTechnology(Group)Co.,Ltd. | 2025-11-04 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84008-003-01 | Pain Relief Gel-Tube | 73 mL in 1 BOTTLE | GEL | 73 | 1 | |
| 84008-003-02 | Pain Relief Gel-Tube | 1 in 1 BOX | GEL | 1 | 1 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.