Phquirogel
FDA Label NDC 70544-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Issislen Laboratori S.l. for the product Phquirogel (NDC 70544-001). 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, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Camphor (3.01%)

Menthol (2.10%)

Purpose

Pain Relieving

Uses

  • For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains bruises and sprains.

Warnings

For external use only

Do Not Use

  • on wounds or damaged skin
  • with a bandage to cover the surface

When Using This Product

  • avoid contact with the eyes

Stop Use And Ask A Doctor If

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep Out Of Reach Of Children.

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

Directions

  • Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 6 years of age: Consult a doctor.

Inactive Ingredients

ALCOHOL DENAT., BENZYL ALCOHOL, CARBOMER, DISODIUM EDTA, FD&C BLUE NO.1, FD&C YELLOW NO.5, GLYCERIN, GINSENG, PEG-7 GLYCERYL COCOATE, PHENOXYETHANOL, POTASSIUM SORBATE, SODIUM BENZOATE, SODIUM CHLORIDE, TOCOPHEROL, TRIETHANOLAMINE,
WATER.

Package Labeling:

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