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 table
LabelManufacturerEffective dateType
ROCKTAPE GO Kinesiology Tape and Analgesic - Implus Footcare, LLCImplus Footcare, LLC2026-01-29HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81683-002-01ROCKTAPE GO Kinesiology Tape and Analgesic1 in 1 BOXSOLUTION200 mg in 1mL2
81683-002-01ROCKTAPE GO Kinesiology Tape and Analgesic1 in 1 BLISTER PACKSOLUTION200 mg in 1mL2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81683-002ROCKTAPE GO KINESIOLOGY TAPE AND ANALGESIC (MENTHOL, METHYL SALICYLATE) KIT [IMPLUS FOOTCARE, LLC]1Unmatched20250501_b779c7d8-dbe6-472f-9282-6cced25cfd2e.zip