Home NDC 81683-002
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 Package Descriptions# Package NDC, Product, Description table 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# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81683-002 ROCKTAPE GO KINESIOLOGY TAPE AND ANALGESIC (MENTHOL, METHYL SALICYLATE) KIT [IMPLUS FOOTCARE, LLC] 1 Unmatched 20250501_b779c7d8-dbe6-472f-9282-6cced25cfd2e.zip