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Sooth-a-sting - Medication Information

Product NDC Code 50332-0048
Drug Name

Sooth-a-sting

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine .06 g/g
Isopropyl alcohol .6 g/g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 895749
Application Number M
Labeler Name HART Health
Packages
Package NDC Code Description
50332-0048-1 10 packet in 1 box (50332-0048-1) / .35 g in 1 packet
50332-0048-7 100 packet in 1 package (50332-0048-7) / .35 g in 1 packet
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Benzocaine 6% Isopropyl Alcohol 60%

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 Adults and chldren 2 years of age and older: remover stinger carefully gently wipe on and around point of insect puncture do not reuse wipe dispose of wipe properly Children under 2 years of age: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Water

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 Temporarily relief of pain and itching associated with insect bites insect stings

Purpose

Information about the drug product’s indications for use.
Purpose Topical Anesthetic Topical Antiseptic

Spl product data elements

Usually a list of ingredients in a drug product.
Sooth-a-Sting BENZOCAINE, ISOPROPYL ALCOHOL BENZOCAINE BENZOCAINE ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL WATER

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.
5337StingWipev21f.jpg

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 more than 3 to 4 times daily in or near the eyes or over large portions of the body

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 1-800-222-1222

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 symptoms last more than 3 days unusual redness, swelling, rash, or other irriation occurs

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 do not get in eyes not for prolonged use FLAMMABLE keep away from heat and flame Allergy alert: A severe allertic reaction to insect bites and stings may require life support measures. In such cases, immediately call 911 or your local emergency provider.

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