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Sting relief - Medication Information

Product NDC Code 72459-282
Drug Name

Sting relief

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 60 mg/g
Isopropyl alcohol 600 mg/g
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 895749
Application Number M017
Labeler Name Yiwu Ori-Power Medtech Co.,Ltd.
Packages
Package NDC Code Description
72459-282-00 .34 g in 1 pouch (72459-282-00)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Benzocaine 6% w/v, Isopropyl Alcohol 60% w/v Purpose For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.

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 no more than 3 to 4 times daily. For children under 2 years of age, consult physician before use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Purified Water, Sodium Bicarbonate.

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.
Use Temporary relief for minor burns, scrapes and insect bites.

Purpose

Information about the drug product’s indications for use.
Purpose For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.

Spl product data elements

Usually a list of ingredients in a drug product.
Sting Relief BENZOCAINE, ISOPROPYL ALCOHOL WATER SODIUM BICARBONATE 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.
Package Labeling: Label2

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 Storage Store at room temperature 15°C - 30°C (59°F - 86°F).

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 on broken skin, deep puncture wounds.

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 swallowing, seek medical help and contact poison control immediately.

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 Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops, consult physician. Do not use on broken skin, deep puncture wounds. Keep Out Of Reach Of Children In case of accidental swallowing, seek medical help and contact poison control immediately. Do not use on broken skin, deep puncture wounds.

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