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If a reaction to NEOSALUS FOAM suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued and the prescribing healthcare practitioner consulted. NEOSALUS FOAM should be rubbed gently into the skin until it is completely absorbed.

Depress ridged portion of dispenser, as illustrated at right. HOW SUPPLIED NEOSALUS FOAM is supplied in a 200 gram aerosolized canister bearing the NDC Number 23710-000-02, a 70 gram aerosolized canister bearing the NDC Number 23710-000-70, and a 10 gram aerosolized canister bearing the NDC Number 23710-000-01.

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Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner. DOSAGE AND ADMINISTRATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. Shake canister vigorously before each use. PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner.

Report Problems to the Food and Drug Administration You are encouraged to report negative side effects of prescription drugs to the FDA. CONTRAINDICATIONS Known hypersensitivity to any of the NEOSALUS FOAM ingredients. Avoid contact with the eyes, lips, and other mucous membranes. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided. KEEP THIS AND OTHER MEDICATIONS OUT OF THE REACH OF CHILDREN.

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Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine. DESCRIPTION NEOSALUS CREAM is a fragrance-free, non-comedogenic water soluble dressing formulated for the management of various types of dermatoses, including atopic dermatitis and allergic contact dermatitis. PRECAUTIONS NEOSALUS FOAM is to be used only as directed by a healthcare practitioner. Manufactured for : Quinnova Pharmaceuticals LLC.

It should not be used to treat any condition other than that for which it is prescribed. DOSAGE AND ADMINISTRATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. Manufactured for : Quinnova Pharmaceuticals LLC. Avoid contact with the eyes, lips, and other mucous membranes.

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Depress ridged portion of dispenser, as illustrated at right. Depress ridged portion of dispenser, as illustrated at right. If a reaction to NEOSALUS FOAM suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued and the prescribing healthcare practitioner consulted. DESCRIPTION NEOSALUS CREAM is a fragrance-free, non-comedogenic water soluble dressing formulated for the management of various types of dermatoses, including atopic dermatitis and allergic contact dermatitis. Report Problems to the Food and Drug Administration You are encouraged to report negative side effects of prescription drugs to the FDA. PRECAUTIONS NEOSALUS FOAM is to be used only as directed by a healthcare practitioner.

KEEP THIS AND OTHER MEDICATIONS OUT OF THE REACH OF CHILDREN. DESCRIPTION NEOSALUS CREAM is a fragrance-free, non-comedogenic water soluble dressing formulated for the management of various types of dermatoses, including atopic dermatitis and allergic contact dermatitis. CONTRAINDICATIONS Known hypersensitivity to any of the NEOSALUS FOAM ingredients. CONTRAINDICATIONS Known hypersensitivity to any of the NEOSALUS FOAM ingredients.

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Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine. NEOSALUS FOAM should be rubbed gently into the skin until it is completely absorbed. DOSAGE AND ADMINISTRATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided. PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. Avoid contact with the eyes, lips, and other mucous membranes.

It should not be used to treat any condition other than that for which it is prescribed. Report Problems to the Food and Drug Administration You are encouraged to report negative side effects of prescription drugs to the FDA. NEOSALUS FOAM should be rubbed gently into the skin until it is completely absorbed.

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Shake canister vigorously before each use. KEEP THIS AND OTHER MEDICATIONS OUT OF THE REACH OF CHILDREN. PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. It should not be used to treat any condition other than that for which it is prescribed. Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner. Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner.

If a reaction to NEOSALUS FOAM suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued and the prescribing healthcare practitioner consulted. Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine. Shake canister vigorously before each use. PRECAUTIONS NEOSALUS FOAM is to be used only as directed by a healthcare practitioner. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided.

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HOW SUPPLIED NEOSALUS FOAM is supplied in a 200 gram aerosolized canister bearing the NDC Number 23710-000-02, a 70 gram aerosolized canister bearing the NDC Number 23710-000-70, and a 10 gram aerosolized canister bearing the NDC Number 23710-000-01. Manufactured for : Quinnova Pharmaceuticals LLC. HOW SUPPLIED NEOSALUS FOAM is supplied in a 200 gram aerosolized canister bearing the NDC Number 23710-000-02, a 70 gram aerosolized canister bearing the NDC Number 23710-000-70, and a 10 gram aerosolized canister bearing the NDC Number 23710-000-01. If a reaction to NEOSALUS FOAM suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued and the prescribing healthcare practitioner consulted. Depress ridged portion of dispenser, as illustrated at right. Shake canister vigorously before each use.

KEEP THIS AND OTHER MEDICATIONS OUT OF THE REACH OF CHILDREN. PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. It should not be used to treat any condition other than that for which it is prescribed. Report Problems to the Food and Drug Administration You are encouraged to report negative side effects of prescription drugs to the FDA. Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner. Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine.

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DESCRIPTION NEOSALUS CREAM is a fragrance-free, non-comedogenic water soluble dressing formulated for the management of various types of dermatoses, including atopic dermatitis and allergic contact dermatitis. DOSAGE AND ADMINISTRATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine. KEEP THIS AND OTHER MEDICATIONS OUT OF THE REACH OF CHILDREN.

Shake canister vigorously before each use. Report Problems to the Food and Drug Administration You are encouraged to report negative side effects of prescription drugs to the FDA. Depress ridged portion of dispenser, as illustrated at right.

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PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. PATIENT INFORMATION Directions For Use Apply to affected area three times a day unless otherwise directed by a prescribing healthcare practitioner. If a reaction to NEOSALUS FOAM suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued and the prescribing healthcare practitioner consulted.

Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner. Caution: Federal Law restricts this device to sale by, or on the order of a licensed healthcare practitioner. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided. HOW SUPPLIED NEOSALUS FOAM is supplied in a 200 gram aerosolized canister bearing the NDC Number 23710-000-02, a 70 gram aerosolized canister bearing the NDC Number 23710-000-70, and a 10 gram aerosolized canister bearing the NDC Number 23710-000-01.

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PRECAUTIONS NEOSALUS FOAM is to be used only as directed by a healthcare practitioner. It should not be used to treat any condition other than that for which it is prescribed. Depress ridged portion of dispenser, as illustrated at right. CONTRAINDICATIONS Known hypersensitivity to any of the NEOSALUS FOAM ingredients. Avoid contact with the eyes, lips, and other mucous membranes. Avoid contact with the eyes, lips, and other mucous membranes.

CONTRAINDICATIONS Known hypersensitivity to any of the NEOSALUS FOAM ingredients. NEOSALUS FOAM should be rubbed gently into the skin until it is completely absorbed. Ingredients Carbomer, dimethicone, ethylparaben, glycerin, methylparaben, phenoxyethanol, polysorbate 20, povidone, propylene glycol, propylparaben, purified water, sodium hydroxide, stearic acid, trolamine. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided.