Arthritis Pain Relieving Cream
FDA Label NDC 51367-036

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by International Nature Nutraceuticals, Inc. for the product Arthritis Pain Relieving Cream (NDC 51367-036). 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, uses, warnings, do not use, when using this product, stop using and consult with doctor if:, keep out of reach of children to avoid accidental poisoning, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Menthol- 16%

Methyl Salicylate- 26%

Uses

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

  • Simple backache
  • Sprains
  • Bruises
  • Arthritis

Warnings

For external use only

Do Not Use

  • On wounds
  • On the face
  • Damaged or irritated skin
  • Otherwise than as directed

When Using This Product

  • Avoid contact with the eyes, mouth or mucous membranes
  • Do not bandage tightly

Stop Using And Consult With Doctor If:

  • Condition worsens
  • Symptoms persist for more than 7 days or clear up and occur again within a few days.
  • Use with caution if you are allergic to ingredients

Keep Out Of Reach Of Children To Avoid Accidental Poisoning

Other Information

Keep bottle tightly closed, store in a cool place

If swallowed, get medical help or contact poison control center immediately 

Directions

  • Adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily, children under 2 years of age: Do not use, consult a doctor

Inactive Ingredients

Petrolatum, Eucalyptus Oil, Lanolin Oil, Paraffin

Package

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