Active Ingredients
Menthol 5.64%
Methyl Salicylate 12.5%
Neotica
FDA Label NDC 72398-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lost Tree Health, Llc for the product Neotica (NDC 72398-000). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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)
Label (Label)
Package Labeling: Neotica Creme, 60G (72398-000-01)
Label2 (Label2)
Package Labeling: Neotica Creme, 100G (72398-000-02)
Label3 (Label3)
* Please review the disclaimer below.
