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Neosalus Generic Name & Formulations
Legal Class
Rx
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
Manufacturer
Generic Availability
NO
Neosalus Indications
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
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
