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Sting relief swab - Medication Information

Product NDC Code 82749-010
Drug Name

Sting relief swab

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine .12 g/.6ml
Menthol, unspecified form .006 g/.6ml
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 1037117
Labeler Name Epic Medical Supply Corp
Packages
Package NDC Code Description
82749-010-01 6 ml in 1 carton (82749-010-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients (each swab) Benzocaine USP (20%), L-Menthol USP (1%)

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 Reverse cardboard sleeve then crush at dot between thumb and forefinger. Once solution has saturated tip, apply topically to the sting or bite. May be used on affected area(s) up to 4 times per day.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients D&C Green Dye #5, D&C Yellow Dye #10, FD&C Blue Dye #1, PEG 300 NF, Isopropyl Alcohol USP, Purified Water USP.

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 For temporary relief of pain and itching associated with insect bites and stings.

Purpose

Information about the drug product’s indications for use.
Purpose analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Sting Relief Swab Benzocaine POLYETHYLENE GLYCOL 300 MENTHOL, UNSPECIFIED FORM MENTHOL WATER FD&C BLUE NO. 1 ISOPROPYL ALCOHOL D&C GREEN NO. 5 BENZOCAINE BENZOCAINE D&C YELLOW NO. 10

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.
Packaging Package

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. Not for use with children less than 2 years old without medical advice. If swallowed, get medical help immediately or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Store at room temperature away from light.

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 use in the eyes not for prolonged use do not apply other medications to the same affected areas unless advised by a doctor Stop use and ask a doctor if condition for this preparation is used persists, or if a rash, irritation or allergic reaction develops.

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