Sohm Pain Away Cream
FDA Label NDC 50405-020

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sohm, Inc for the product Sohm Pain Away (NDC 50405-020). 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, directions, other information, inactive ingredients, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Menthol 1.5%
Camphor 4%

Purpose

Menthol 1.5%......................................................External Analgesic
Camphor 4%....................................................... External Analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:
 simple backache
 arthritis
 strains
 bruises
 sprains

Warnings

  • If you have senstive skin, test this product on a small area of skin before applying it to a large area
  • For external use only.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Children under 2 years of age: Do not use, consult a physician

Other Information

store at 20–25°C (68–77°F)

Inactive Ingredients

Water, Glycerin, Sodium Lauryl Sulfate, Glycolic acid, Vitamin E Acetate, Coconut Oil, Cetyl Alcohol, Stearyl Alcohol, sodium metabisulfite.

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