Label: DIABETIC TUSSIN SORE THROAT CHERRY- phenol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 2, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Phenol 1.4%

  • Purpose

    Oral anesthetic/Analgesic

  • Uses

    for the temporary relief of occasional minor irritation, pain, sore mouth and sore throat.

  • Warnings

    Sore Throat Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious.

    Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age unless directed by a doctor.

    When using this product,

    do not exceed recommended dose.

    Stop use and ask a doctor or dentist if

    • sore mouth symptoms do not improve in 7 days
    • irritation, pain or redness persists or worsens
    • swelling, rash or fever develops

    If pregnant or breast-feeding,

    ask a health care professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Adults and children 12 years of age and older:

    • Apply to the affected area (one spray).
    • Allow to remain in place for at least 15 seconds, then spit out.
    • Use every 2 hours or as directed by a doctor or dentist.

    Children under 12 years of age: ask a doctor before use.

  • Other information

    • store between 20°-25°C (68-°77°F). 
    • do not refrigerate.
  • Inactive ingredients

    alcohol, FD&C red #40, flavors, glycerin, purified water, sodium saccharin anhydrous

  • Questions?

    1-800-579-8327

  • Principal Display Panel

    Diabetic Tussin®
    Phenol / Oral Pain Reliever
    Cherry
    6 fl oz (177 mL) SPRAY

    Diabetic Tussin® Phenol / Oral Pain Reliever Cherry 6 fl oz (177 mL) SPRAY

  • INGREDIENTS AND APPEARANCE
    DIABETIC TUSSIN SORE THROAT CHERRY 
    phenol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61787-066
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL1.4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61787-066-06177 mL in 1 BOTTLE; Type 0: Not a Combination Product06/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02206/20/2024
    Labeler - MEDTECH PRODUCTS INC (114707784)
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