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Age intervention duality - Medication Information

Product NDC Code 65113-2372
Drug Name

Age intervention duality

Type Brand
Active Ingredients
Benzoyl peroxide 10 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 106315
Application Number part333D
Labeler Name G.S. COSMECEUTICAL USA, INC.
Packages
Package NDC Code Description
65113-2372-2 28 g in 1 bottle, pump (65113-2372-2)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Benzoyl Peroxide-10%

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 Clean the skin thoroughly before applying this product. This product contains two parts. Dispense equal quantities of product from each of the two pumps, then briefly mix the two parts together on your palm. Cover the entire affected area with a thin layer one to three times daily. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a physician. If bothersome dryness or peeling occurs, reduce application to once a day or every other day. If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Water (Aqua), Propylene Glycol, Glycerin, Sorbitol, Polyacrylamide, C13-14 Isoparaffin, Cyclopentasiloxane, Cyclohexasiloxane, Carbomer, Laureth 7, Disodium EDTA, Triethanolamine, Diazolidinyl Urea, Methylparaben, Propylbaraben

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 For the treatment of Acne. Reduces the severity of acne blemishes, acne pimples, blackheads, whiteheads and allows the skin to heal.

Purpose

Information about the drug product’s indications for use.
Purpose Anti-acne

Spl product data elements

Usually a list of ingredients in a drug product.
AGE INTERVENTION DUALITY BENZOYL PEROXIDE BENZOYL PEROXIDE BENZOYL PEROXIDE WATER GLYCERIN GLYCERYL STEARATE CITRATE POLYSORBATE 20 POLYSORBATE 60 STEARYL ALCOHOL RETINOL SORBITOL CAMELLIA OLEIFERA LEAF PALMITOYL TETRAPEPTIDE-7 PALMITOYL HEXAPEPTIDE-12 CHRYSIN DIMETHICONE STEARETH-20 PHENOXYETHANOL HEXYLENE GLYCOL ETHYLHEXYLGLYCERIN CAPRYLYL GLYCOL VERY PALE YELLOW

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.
PRINCIPAL DISPLAY PANEL - 28 g Carton AGE INTERVENTION ® DUALITY ™ Benzoyl Peroxide 10% Adult Acne Treatment Cream and Anti-Aging Complex JANMARINI SKIN RESEARCH ® 28 g / 1 oz. PRINCIPAL DISPLAY PANEL - 28 g Carton

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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you have very sensitive skin are sensitive to benzoyl peroxide

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If accidentally swallowed, seek medical help immediately or contact the Poison Control Center.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a physician if irritation becomes severe

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. When using this product avoid unnecessary sun exposure and use a sunscreen avoid contact with hair and dyed fabrics, which may be bleached by this product avoid contact with the eyes, lips and mouth skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration

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. When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Do not use if you have very sensitive skin are sensitive to benzoyl peroxide When using this product avoid unnecessary sun exposure and use a sunscreen avoid contact with hair and dyed fabrics, which may be bleached by this product avoid contact with the eyes, lips and mouth skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration Stop use and ask a physician if irritation becomes severe Keep out of reach of children. If accidentally swallowed, seek medical help immediately or contact the Poison Control Center.

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