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| Product NDC Code | 65517-0005 | ||||
|---|---|---|---|---|---|
| Drug Name | Dukal sting relief pad |
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| Type | Brand | ||||
| Pharm Class | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
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| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SWAB | ||||
| RxCUI drug identifier | 895749 | ||||
| Application Number | M003 | ||||
| Labeler Name | Dukal LLC | ||||
| 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.Active Ingredients Benzocaine, 6% w/v Isopropyl Alcohol 60% w/v
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 Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years; consult physician.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredient Purified Water D07110607 Rev5
Purpose
Information about the drug product’s indications for use.Purpose Topical Anesthetic Antiseptic
Spl product data elements
Usually a list of ingredients in a drug product.DUKAL STING RELIEF PAD BENZOCAINE WATER BENZOCAINE BENZOCAINE ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL
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 - 0.4 mL Pouch Label DUKAL ™ CORPORATION REF 856 NDC 65517-0005-1 STING RELIEF PAD For temporary relief of pain and itching associated with minor burns, scrapes and insect bites. For External Use Only 1 Pouch DUKAL CORPORATION • (631) 656-3800 Ronkonkoma, New York • www.dukal.com Made in China, Hecho en China, Fabriqué en Chine Principal Display Panel - 0.4 mL Pouch 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.Do Not Use In the eyes. If contact occurs, rinse thoroughly with water
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 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.Stop Use If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse. Caution Flammable
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.Do Not Use In the eyes. If contact occurs, rinse thoroughly with water Stop Use If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse. Caution Flammable Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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