• Atopic dermatitis

Neosalus Generic Name & Formulations

General Description

Dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, stearic acid, trolamine, butane and propane (propellants); foam; fragrance-free.

Pharmacological Class

Antipruritic (nonsteroidal).

See Also

    How Supplied

    Foam—10g, 70g, 200g; Crm—60g, 100g; Lotion—236mL


    Generic Availability


    Neosalus Indications


    Dermatitis (eg, atopic dermatitis, contact dermatitis).

    Neosalus Dosage and Administration

    Adults and Children

    Apply to affected areas 3 times daily or as needed.

    Neosalus Contraindications

    Not Applicable

    Neosalus Boxed Warnings

    Not Applicable

    Neosalus Warnings/Precautions


    Avoid contact with eyes, lips, angles of the nose, and mucous membranes. Discontinue if sensitivity or irritation occurs. Avoid exposure to sun or UV light.

    Neosalus Pharmacokinetics

    See Literature

    Neosalus Interactions

    Not Applicable

    Neosalus Adverse Reactions

    Adverse Reactions

    Erythema, dryness, scaling, burning, pruritus.

    Neosalus Clinical Trials

    See Literature

    Neosalus Note

    Not Applicable

    Neosalus Patient Counseling

    See Literature