Dosage and administration
-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.
Neuraxacin Neuromethacin
- Manufacturer
- Sola Pharmaceuticals
- Effective date
- 2020-12-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:57:33
Label at a glance#
ProductNeuraxcin Neuromethacin
Active ingredientMENTHOL
Label structure10 sections
Storage and handling
Store at room temperature.
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Menthol
OTC - PURPOSE SECTION
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 LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70512-105-90 | 2022-12-12 | C162847 | 48780-1 | d6a99b39-9b66-a426-e053-dadaa90af4c2 | Neuraxcin Neuromethacin, Pain Relief Roll-on |
| 70512-105-90 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-9b66-a426-e053-dadaa90af4c2 | Neuraxcin Neuromethacin, Pain Relief Roll-on |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70512-105-90 | ML - Milliliter | 70512-105 | 1c5d295c-0c29-478b-9b0a-687bd5497812 | 1 | 2021-03-02 |
Products#
Every source-derived product name is available through these pages.
- Neuraxcin Neuromethacin
- Menthol Roll-on
- ALOE VERA LEAF
- PHENOXYETHANOL
- MENTHOL
- GLYCERIN
- ISOPROPYL MYRISTATE
- DIMETHYL SULFONE
- WATER
- INDIAN FRANKINCENSE
- ISOPROPYL ALCOHOL
- GREEN TEA LEAF
- GLYCERYL MONOSTEARATE
- ARNICA MONTANA FLOWER
- HELIANTHUS ANNUUS FLOWERING TOP
- CETYL ALCOHOL
- GLUCOSAMINE SULFATE
- CAPRYLYL GLYCOL
- XANTHAN GUM
- CITRIC ACID MONOHYDRATE
- STEARIC ACID
- CETEARYL OLIVATE
- SORBITAN OLIVATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70512-105 | 70512-105-90 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| efa595a0-532d-d1b9-e053-2a95a90a1036 | b6239df0-a778-479c-e053-2a95a90a6ab5 | 2022-12-12 | Warnings | b6239df0-a778-479c-e053-2a95a90a6ab5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.