NEUROLATORE POWER FORMULA PAIN RELIEF- methyl salicylate, menthol cream

Neurolatore Power Formula Pain Relief by

Drug Labeling and Warnings

Neurolatore Power Formula Pain Relief by is a Otc medication manufactured, distributed, or labeled by Miracle Breakthrough Labs Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Methyl Salicylate 18.50%

Menthol 9%

Purpose

Topical Analgesic

Indications:

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

Warnings:

Always consult a physician before use.  For external use only.  Avoid contact with eyes.  If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

If swallowed, consult physician.  Do not apply to wounds or damaged skin.  Do not bandage tightly.

If pregnant or breast feeding,

ask a health professional before use.

Allergy Alert:

If you have had a prior allergic reaction to aspirin or salicylates, please consult physician prior to use.

Directions:

Adults and children two-years of age and older: Apply to affected area not more than three to four times daily.  Children under two-years of age: consult a physician.

Other information:

Store at room temperature.

Inactive ingredients:

Allantoin, Aqua (Deionezed Water), Boswella Serrata Extract, Caprylic/Capric Triglyceride, Capsaicin, Cetearyl Alcohol, Cetearyl Olivate, Curcuma Longa (Turmeric) Extract, Dimethyl Sulfoxide (DMSO), Ethylhexylglycerin, Glycerin, Harpagophytum Procumbens (Devil’s Claw) Root Extract, Isopropyl Myristate, Phenoxyethanol, Salix Alba (Willow) Bark Extract, Sodium Alginate, Sodium Lauryl Sulfate, Sodium Polyacrylate, Sorbitan Olivate, Sunflower Wax.

Package Labeling:

INGREDIENTS AND APPEARANCE

NEUROLATORE POWER FORMULA PAIN RELIEF 
methyl salicylate, menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70584-734
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	185 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	90 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CAPSAICIN (UNII: S07O44R1ZM)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
TURMERIC (UNII: 856YO1Z64F)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SALIX ALBA BARK (UNII: 205MXS71H7)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SORBITAN OLIVATE (UNII: MDL271E3GR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70584-734-01	57 g in 1 JAR; Type 0: Not a Combination Product	02/07/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/29/2016

Labeler - Miracle Breakthrough Labs Corporation (177008146)