Label: STING AND BITE- benzocaine swab

  • NDC Code(s): 60913-031-01
  • Packager: PHOENIX HEALTHCARE SOLUTIONS, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient

    Benzocaine, 6% w/v

  • Purpose

    Topical Analgesic

  • Use

    For temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes and insect bites or minor skin irritations.

  • Warnings

    • For external use only.
    • Flammable, keep away from fire or flame
    • Avoid contact with eyes; if this happens, rinse thoroughly with water

    Do Not Use

    With electrocautery procedures.

    Stop Use

    If irritation and redness develop.If condition worsens or if symptoms persist for more than 7 days, or clear up and occur again within a few days,discontinue use and consult a doctor.

    Caution:Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • For adults and children 2 years of age and older, apply to affected area not more than 3-4 times daily.
    • For children under 2 years of age, consult a doctor before use.
  • Other information

    Store at room temperature 15 0 -30 0 C (59 0 - 86 0 F). Avoid excessive heat.

  • Inactive ingredients

    Isopropyl Alcohol, Purified Water

  • Principal Display Panel

    NDC 60913-031-01

    Phoenix Healthcare Solutions, LLC

    "An Innovative Medical Manufacturer"

    Sting and Bite Pads

    Medium

    For Individual,Professional and Hospital Use

    Saturated with 6% Benzocaine as a topical analgesic

    Latex Free

    100 Individual Pads

    Label

  • INGREDIENTS AND APPEARANCE
    STING AND BITE 
    benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60913-031
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60913-031-01100 in 1 CARTON02/23/2015
    11 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/23/2015
    Labeler - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!