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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.