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Product NDC Code | 50157-609 | ||||
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Drug Name | Deep cleansing foaming acne scrub |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | LIQUID | ||||
Application Number | part358H | ||||
Labeler Name | Brands International Corporation | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Salicylic Acid 2.0%.
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.Direction use twice daily apply water to face and hands dispense our product into hands and lather apply to face, nose, and neck, and gently massage into skin rinse thoroughly with tepid water
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Hydroxymethyl cellulose, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Walnut Shell Powder, Vitamin E, Aloe Vera Leaf Extract.
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.Indications and Use For management of Acne
Purpose
Information about the drug product’s indications for use.Acne Treatment
Spl product data elements
Usually a list of ingredients in a drug product.Deep cleansing foaming acne scrub Salicylic Acid WATER SODIUM LAURETH SULFATE COCAMIDOPROPYL BETAINE SODIUM LAURYL SULFATE HYDROXYMETHYL CELLULOSE DITETRACYCLINE TETRASODIUM EDETATE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE BLACK WALNUT SHELL VITAMIN E POLYETHYLENE GLYCOL SUCCINATE SALICYLIC ACID SALICYLIC ACID ALOE VERA LEAF
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.1
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 In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Store at room temperature.
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 doctor if irritation or redness develops
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.
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.For external use only Avoid contact with eyes. If contact occurs, flush thoroughly with water
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