Label: STING RELIEF PAD- benzocaine, isopropyl alcohol patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 13, 2017

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

View All Sections
  • Active Ingredient

    Benzocaine 6.0% w/v

    Isopropyl Alcohol 70.0% v/v

    Purpose

    Topical Analgesic

    Antiseptic

  • Uses

    Prevent infection in minor scrapes and temporary relief of itching of insect bites

  • Warnings

    -For external use only

    -Caution Flammable

    -Do Not Use in the eyes. If contact occurs, rinse throughly with water.

    -Stop Use if irritation, redness or other symptoms develop. Consult a doctor if condition persist or gets worse.

    Keep out of reach of children.

    If swallowed, get medical help or contact a poison control center right away.

  • Directions

    Apply to affected area 3 or 4 times daily.

    For Adults and children 2 years of age and older.

    Children under 2 years: consult physician.

  • Inactive Ingridients

    Purified Water

  • Label

    image description

  • INGREDIENTS AND APPEARANCE
    STING RELIEF PAD 
    benzocaine, isopropyl alcohol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44019-911
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.06 g  in 1 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44019-911-010.42 mL in 1 POUCH; Type 0: Not a Combination Product08/23/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/23/2016
    Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
    Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)
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!