ROCKTAPE GO Kinesiology Tape and Analgesic

Manufacturer
Implus Footcare, LLC
Effective date
2026-01-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:35:37

Label at a glance#

ProductROCKTAPE GO Kinesiology Tape and Analgesic
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure7 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.

Dosage and administration

Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily Children under 2 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%
Methyl Salicylate 20%

PURPOSE

OTC - PURPOSE SECTION

Topical Analgesic
Anti-inflammatoire Topique

USES

INDICATIONS & USAGE SECTION

  • For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes
  • Do not apply to wounds or damaged skin
  • Do not bandage tightly

Stop use and ask doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily
  • Children under 2 years of age: do not use, consult a doctor.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

  • Store at 68°F to 77°F (20° to 25°C)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe vera [aloe barbadensis] Leaf Juice, Capsaicin, Carbomer, Cetearyl Alcohol, Dimethyl Silicone Oil, 2-Ethylhexyl Palmitate, Methylparaben, Phenoxyethanol, Polysorbate 60, Propylene Glycol, Propylparaben, Purslane (Portulaca oleracea) Extract, Sorbitan Stearate, Triethanolamine, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package0Outer Package0

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81683-001-01ROCKTAPE GO Kinesiology Tape and Analgesic1 in 1 KITKIT12
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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81683-00181683-001-01
81683-00281683-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ROCKTAPE GO Kinesiology Tape and AnalgesicMENTHOL, METHYL SALICYLATEImplus Footcare, LLCb779c7d8-dbe6-472f-9282-6cced25cfd2e2026-01-29WarningsExact identifier
ndc (package): 81683-001-01
ndc (package): 81683-002-01
ndc (product): 81683-001
ndc11 (package): 81683000101
ndc11 (package): 81683000201
spl id: 4987e1bd-0b55-74e3-e063-6394a90a63c9
spl set id: b779c7d8-dbe6-472f-9282-6cced25cfd2e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.