Sanar Naturals Camphor Ointment
FDA Label NDC 73386-151

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 Camphor (NDC 73386-151). 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

Topical Analgesic

Uses

Aid for temporary relief of minor pain of muscles or 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. Massage until thoroughly absorbed, repeat as necessary, but not more than 3 times daily.
  • Children under 12 years: Consult a doctor.

Inactive Ingredients

Petrolatum

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