FDA Label for Neotica

View Indications, Usage & Precautions

Neotica Product Label

The following document was submitted to the FDA by the labeler of this product Lost Tree Health, Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredients



Menthol 5.64%

Methyl Salicylate 12.5%


Purpose



External Analgesic


Use



  • For the temporary relief of minor aches and pains of muscles and joints

Warnings



For external use only


When Using This Product



  • use only as directed
  • avoid contact with the eyes and mucous membranes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop Use And Ask A Doctor If



  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • excessive irritation of the skin develops

Keep Out Of Reach Of Children.



If swallowed, get medical help or contact a Poison Control Center right away.


Directions



  • Adults and children 3 years of age and older:  Apply to affected area not more than 3 to 4 times daily.
  • Children under 3 years of age: Consult a doctor.

Other Information



  • Store at temperatures not exceeding 86°F / 30°C

Inactive Ingredients



Carbomer 934, glyceryl monostearate, PEG-20 sorbitan beeswax, sodium hydroxide, sodium lauryl sulfate, water


Package Labeling: Neotica Creme, 15G (72398-000-00)




Package Labeling: Neotica Creme, 60G (72398-000-01)




Package Labeling: Neotica Creme, 100G (72398-000-02)




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