NDC 81683-002 - ROCKTAPE GO Kinesiology Tape and Analgesic
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
- 81683-002
- Package NDCs from labels
- 81683-002-01
- Manufacturer
- Implus Footcare, LLC
- Effective date
- 2026-01-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ROCKTAPE GO Kinesiology Tape and Analgesic - Implus Footcare, LLC | Implus Footcare, LLC | 2026-01-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81683-002-01 | ROCKTAPE GO Kinesiology Tape and Analgesic | 1 in 1 BOX | SOLUTION | 200 mg in 1mL | 2 | |
| 81683-002-01 | ROCKTAPE GO Kinesiology Tape and Analgesic | 1 in 1 BLISTER PACK | SOLUTION | 200 mg in 1mL | 2 |
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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| COLD AND HOT MEDICATED Patch | COLD AND HOT MEDICATED PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49aca763-be2a-cf38-e063-6294a90a092e | 2026-01-31 | Warnings | M017 L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.