Active Ingredient
Camphor 0.5%
Procure Anti Itch Lotion
FDA Label NDC 55681-038
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Twin Med Llc for the product Procure Anti Itch (NDC 55681-038). 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, when using this product, 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
Purpose
External Analgesic
Uses
Uses
For the temporary relief of pain and itching associated with: nsect bites, minor cuts, minor burns, sunburn, scrapes, minor skin irritations, rashes due to poison ivy, poison oak, or poison sumac
Warnings
Warnings
For external use only
When Using This Product
When using this product avoid contact with the eyes
Stop Use And Ask A Doctor If
Stop use and ask a doctor if
- Condition worsens
- Symptoms last more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.
Directions
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
Inactive Ingredients
Inactive Ingredients
Carbomer, Cetostearyl Alcohol, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Imidurea, Glycol Stearate, Menthol, Mineral Oil, PEG-40 Castor Oil, Petrolatum, Phenoxyethanol, Propylene Glycol, Sodium Cetostearyl Sulfate, Sodium Hydroxide, Stearic Acid, Titanium Dioxide, Water
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