Sanar Naturals Arnica Pain Releiving Roll On With Camphor Liquid
FDA Label NDC 73386-148

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sanvall Enterprises, Inc for the product Sanar Naturals Arnica Pain Releiving Roll On With Camphor (NDC 73386-148). 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 ingredient, purpose, uses, warnings, do not, 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

Active Ingredient

Camphor 1%

Purpose

Pain Relief

Uses

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

Warnings

For external use only

Avoid contact with eyes.

Stop Use And Ask A Doctor If

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again.

Keep Out Of Reach Of Children.

is swallowed, get medical help or contact Poison Control Center right away

Directions

  • Adults and children over 12 years: Apply to affected area no more than 3 to 4 times daily.
  • Children under 12 years: Do not use, consult a doctor.

Inactive Ingredients

Aqua, Arnica Montana Flowe Extract, Propylene Glycol, Menthol, Glycerin, Carbomer, Methyl Salicylate, Ththanolamine, Eucalyptus Globulus Leaf Oil, Disodium EDTA, Tocopheryl Acetate, Capsicum Annum Fruit Extract, Methylchloroisothiazolinone, Methylisothiazolinone.

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