Rocktape Go Kinesiology Tape And Analgesic Kit
FDA Label NDC 81683-001
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Implus Footcare, Llc for the product Rocktape Go Kinesiology Tape And Analgesic (NDC 81683-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredients, purpose, uses, warnings, when using this product, stop use and ask doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Menthol 10%
Methyl Salicylate 20%
Purpose
Topical Analgesic
Anti-inflammatoire Topique
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, sprains.
Warnings
FOR EXTERNAL USE ONLY
When Using This Product
- Avoid contact with eyes
- Do not apply to wounds or damaged skin
- Do not bandage tightly
Stop Use And Ask Doctor If
- 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.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- 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
- Store at 68°F to 77°F (20° to 25°C)
Inactive Ingredients
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:
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