Dermeleve Scalp Psoriasis Treatment Liquid
FDA Label NDC 81507-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Advanced Derm Solutions Llc for the product Dermeleve Scalp Psoriasis Treatment (NDC 81507-006). 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, directions, other information, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Salicylic acid 2%

Purpose

Psoriasis

Uses

• For relief of the symptoms of psoriasis
• Controls scalp itch, irritation, redness, flaking, and scaling associated with psoriasis

Warnings

For external use only

When using this product Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

If condition worsens or does not improve after regular use of this product as directed, consult a doctor. If the condition covers a large area of the body, consult your doctor before using this product.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Use a dropper to apply to the affected areas of the scalp one to four times daily or as directed by a doctor
  • Massage into the scalp and leave on for at least 30 minutes for the best results.
  • If applying after shampooing, towel-dry hair first

Other Information

Store below 75°F / 24°C

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Butylene Glycol,Calcium Chloride,Caprylyl Glycol,Citric Acid,Glycerin, Lactic Acid,Phenoxyethanol,Polysorbate 80, Propylene Glycol, Sodium Carbonate, Sodium Hydroxide, Strontium Nitrate,Water, Xanthan Gum

Product Label

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