Active Ingredient
Aluminum acetate (0.2%)
Dermeleve Cream
FDA Label NDC 81507-002
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 (NDC 81507-002). 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, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Astringent
Uses
• Insects Bites
• Minor Burn
• Athlete's foot
• Poison lvy
• Poison oak
• Poison sumac
• Rashes cause by soaps, detergents, cosmetic or jewelry
Warnings
■
For external use only.
■
Avoid contact with eyes.
■
Do not apply to open wounds.
■
STOP USE and ask a doctor if condition worsens
or symptoms persist for more than seven days.
■ Keep out of reach of children.
Directions
Adults and children two years of age and older,
apply to affected area as needed or as directed by a doctor. Consult a doctor for children under the age of two.
Inactive Ingredients
Water, Strontium Nitrate, Isopropyl Myristate, Butyrospermum Parkii (shea) Butter, Caprylyc/Capric Triglyceride, Cetearyl Alcohol, Emulsifying Wax NF, Glycerin, Phenoxyethanol, Magnesium Aluminum Silicate, Glyceryl Stearate, Dimethicone, Polyacrylate Crosspolymer-6, Xanthan Gum, Caprylyl Glycol, Sodium Hyaluronate, Disodium EDTA, Ceramide NG, Tocopherol (Vitamin E), Tetrahexyldecyl Ascorbate
Product Label
Image Description (Label 80gm 2)
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