DERMELEVE SCALP PSORIASIS TREATMENT- salicylic acid liquid

Dermeleve Scalp Psoriasis Treatment by

Drug Labeling and Warnings

Dermeleve Scalp Psoriasis Treatment by is a Otc medication manufactured, distributed, or labeled by Advanced Derm Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

KEEP OUT OF REACH OF CHILDREN

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 75ºF / 24ºC

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

SPL UNCLASSIFIED SECTION

Questions? Visit www.dermeleve.com
or call +1 (877) 684-2299

Manufactured for Advanced Derm Solutions LLC
Oldsmar, FL 34677 | dermeleve.com | +1 (877) 684-2299
U.S. Patents: 5,716,625; 5,804,203; 6,139,850; 7,404,967

Product label

INGREDIENTS AND APPEARANCE

DERMELEVE SCALP PSORIASIS TREATMENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81507-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID (UNII: 33X04XA5AT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CARBONATE (UNII: 45P3261C7T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STRONTIUM NITRATE (UNII: BDG873AQZL)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81507-006-01	1 in 1 BOX	03/19/2026
1		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	03/19/2026

Labeler - Advanced Derm Solutions LLC (117840544)