Label: ZONSEN STING RELIEF PAD- isopropyl alcohol, benzocaine swab

  • NDC Code(s): 72932-004-00
  • Packager: Wuhan Zonsen Medical Products Co., Ltd.
  • 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 May 20, 2019

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  • Drug Facts

  • Active Ingredients

    Isopropyl Alcohol 70%

    Benzocaine 6%

    Purpose

    Antiseptic

    Topical Analgesic

  • Use

    For prevent infection in minor scrape and temporary relief of itching of insect bites

  • Warnings

    • For external use only.
    • Flammable, keep away from fire or flame.

    Do Not Use

    • With electrocautery procedures.
    • In the eyes. If contact occurs, flush eyes with water.

    Stop Use

    if irritation and redness develop. If condition continues, consult your health care practitioner.

    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.
  • Other information

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

  • Inactive Ingredients:

    purified water

  • Package Labeling:

    Label4

  • INGREDIENTS AND APPEARANCE
    ZONSEN STING RELIEF PAD 
    isopropyl alcohol, benzocaine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72932-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE60 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72932-004-001 in 1 POUCH04/01/2019
    10.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2019
    Labeler - Wuhan Zonsen Medical Products Co., Ltd. (554474517)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wuhan Zonsen Medical Products Co., Ltd.554474517manufacture(72932-004)
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