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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| Yeheal | CAMPHOR, MENTHOL, ISOPROPYL ALCOHOL | Shenzhen Yeheal Biotechnology Co., Ltd | 3cf1bc74-3060-6d63-e063-6294a90a9f5c | 2025-08-22 | Warnings | M017 L7T10EIP3A |
| Refresh RELIEVA PF | CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN | Allergan, Inc. | d5d3df4a-a311-4f2d-9a24-edfec1a6c9f9 | 2025-08-22 | Warnings | PDC6A3C0OX |
| Refresh Optive | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Allergan, Inc. | 37e99aa8-02d6-4efb-a862-90bc7fcd5ca5 | 2025-08-22 | Warnings | PDC6A3C0OX |
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| Barrier Protectant Cream | BARRIER CREAM | Cardinal Health | 539d9aac-75cf-4efd-bb3e-b465563304ca | 2025-08-21 | Warnings | L7T10EIP3A |
| SUGARLOAF ORGANICS MENTHOL REVIVE | MENTHOL | RENU LABORATORIES, LLC | fa2f9539-b703-a00b-e053-6394a90ae309 | 2025-08-21 | Warnings | M017 L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.