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Dermeleve anti itch scalp serum - Medication Information

Product NDC Code 81507-004
Drug Name

Dermeleve anti itch scalp serum

Type Brand
Active Ingredients
Aluminum acetate .2 g/100ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 2638676,
2638678
Application Number M016
Labeler Name Advanced Derm Solutions LLC
Packages
Package NDC Code Description
81507-004-01 89 ml in 1 bottle (81507-004-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Aluminum acetate (0.2%)

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children two years of age and older, apply to affected area as needed or as directed by a doctor. Twist the flow-control cap to open. Apply directly to scalp, rub in if needed. Consult a doctor for children under the age of two.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Butylene Glycol, Calcium Chloride, Caprylyl Glycol, Disodium EDTA, Glycerin, Lactic Acid, Niacinamide, Phenoxyethanol, Polysorbate 80, Strontium Nitrate, Water, Xanthan Gum

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Scalp itch; rashes caused by soaps, detergent, or cosmetics

Purpose

Information about the drug product’s indications for use.
Purpose Astringent

Spl product data elements

Usually a list of ingredients in a drug product.
Dermeleve Anti Itch Scalp Serum Aluminum Acetate BUTYLENE GLYCOL CALCIUM CHLORIDE CAPRYLYL GLYCOL EDETATE DISODIUM ANHYDROUS GLYCERIN LACTIC ACID NIACINAMIDE PHENOXYETHANOL POLYSORBATE 80 STRONTIUM NITRATE WATER XANTHAN GUM ALUMINUM ACETATE ALUMINUM CATION

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
image description image description image description image description image description image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Store at 20-25ºC (68-77ºF). Keep carton for full product information Questions? Visit www.dermeleve.com or call 877-684-2299

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API