Neuraxcin Neuromethacin, Pain Relief Roll-on

Neuraxcin Neuromethacin by

Drug Labeling and Warnings

Neuraxcin Neuromethacin by is a Otc medication manufactured, distributed, or labeled by Sola Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEURAXCIN NEUROMETHACIN- menthol roll-on liquid 
Sola Pharmaceuticals

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neuraxcin Neuromethacin, Pain Relief Roll-on

Menthol

Topical Analgesic

Indications

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

Warnings

-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

Contact physician prior to use.

Directions

-Adults and children two-years of age or older. Apply to affected area not more than three to four times daily.

-Children under two-years of age, consult a physician.

Storage

Store at room temperature.

Other Ingredients

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montant Flower Extract, Boswellia Serrata Extract, Camellia Sinensis (Green Tea) Extract, Cannabis Sativa (Full Spectrum Hemp) Oil, Caprylyl Glycol, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Helianthus Annus (Sunflower) Oil, Isopropyl Alcohol, Isopropyl Myristate, Methylsufonylmethane (MSM), Phenoxyethanol, Sorbitan Olivate, Stearic Acid, Xanthan Gum.

Package labeling

NEURAXCIN NEUROMETHACIN 
menthol roll-on liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70512-105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
WATER (UNII: 059QF0KO0R)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70512-105-9090 mL in 1 BOTTLE; Type 0: Not a Combination Product12/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/10/202012/12/2022
Labeler - Sola Pharmaceuticals (080121345)

Revised: 12/2022
 

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