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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| SUGARLOAF ORGANICS MENTHOL REVIVE | MENTHOL | RENU LABORATORIES, LLC | fa2f9539-b703-a00b-e053-6394a90ae309 | 2025-08-21 | Warnings | M017 L7T10EIP3A |
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| Capsaicin 0.035% Cream | CAPSAICIN 0.035% CREAM | Puretekcorp | 3cbc73b6-8c58-8f23-e063-6394a90a71a3 | 2025-08-20 | Warnings | M017 S07O44R1ZM |
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| Game On | MENTHOL, METHYL SALICYLATE | Natural Essentials, Inc. | 3cd20f1f-033f-f698-e063-6294a90a89eb | 2025-08-20 | Warnings | M017 L7T10EIP3A LAV5U5022Y |
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| Hydrocortisone | HYDROCORTISONE SPRAY | FSA Store Inc. | 3ce24b87-55ac-0bbd-e063-6294a90ab582 | 2025-08-19 | Warnings | M017 |
| Fast Freeze Pain Relieving | MENTHOL, UNSPECIFIED FORM | NATURAL ESSENTIALS, INC. | 15a26af1-ca5a-40fc-a411-6c0e8ae18fbb | 2025-08-18 | Warnings | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.