ROCKTAPE GO KINESIOLOGY TAPE AND ANALGESIC- menthol, methyl salicylate kit

ROCKTAPE GO Kinesiology Tape and Analgesic by

Drug Labeling and Warnings

ROCKTAPE GO Kinesiology Tape and Analgesic by is a Otc medication manufactured, distributed, or labeled by Implus Footcare, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

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:

INGREDIENTS AND APPEARANCE

ROCKTAPE GO KINESIOLOGY TAPE AND ANALGESIC 
menthol, methyl salicylate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81683-001

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81683-001-01	1 in 1 KIT	05/01/2025

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	49.3 mL

Part 1 of 1

ROCKSAUCE ROLL ON EXTERNAL ANALGESIC 
menthol, methyl salicylate solution

Product Information
Item Code (Source)	NDC: 81683-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPSAICIN (UNII: S07O44R1ZM)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
PURSLANE (UNII: M6S840WXG5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81683-002-01	1 in 1 BOX
1		1 in 1 BLISTER PACK
1		49.3 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/01/2025

Labeler - Implus Footcare, LLC (361531585)