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Product NDC Code | 84445-008 | ||||
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Drug Name | Corn care patches |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | PATCH | ||||
RxCUI drug identifier | 2688287 | ||||
Application Number | M030 | ||||
Labeler Name | Shenzhen Furuizhilian keji Co., Ltd. | ||||
Packages |
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Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Salicylic acid 15%
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.■ wash affected area and dry thoroughly ■ let dry ■ attach the patch to the affected area ■ repeat procedure once or twice daily as needed for up to 14 days (until corn/callus is removed) ■ may soak corn/callus in warm water for 5 minutes to assist in removal ■ protective pads may be used to cushion corn/callus during treatment Children under 12 years of age: consult a doctor
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.safflower, stemona, borneol, camphor
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.■ for the removal of corns and calluses ■ relieves pain by removing corns and calluses
Purpose
Information about the drug product’s indications for use.Corn and callus remover
Spl product data elements
Usually a list of ingredients in a drug product.CORN CARE PATCHES Salicylic acid STEMONA TUBEROSA ROOT BORNEOL SALICYLIC ACID SALICYLIC ACID CAMPHOR, (-)- SAFFLOWER
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.label
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.■ if you have diabetes ■ if you have poor blood circulation ■ on irritated skin or any area that is infected or reddened
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.If swallowed, get medical help or contact a Poison Control Center right away.
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.discomfort lasts
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.■ if product gets in eyes, flush with water for 15 minutes ■ do not inhale vapors ■ store at room temperature away from heat
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 ■ Flammable: Keep away from fire or flame.
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