Label: SYREN INTIMATE PAIN RELIEF- lidocaine hydrochloride gel

  • NDC Code(s): 69233-122-02
  • Packager: Icon Health Science, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active Ingredients

    Lidocaine hydrochloride 4%

    Purpose

    Topical Analgesic

  • Uses:

    • For the temporary relief of pain (and itching) associated with minor, burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations.
  • Warnings:

    For external use only.

    Do not use

    • in large quantities, particularly over raw surfaces or blistered areas.

    When using this product

    • Avoid contact with the eyes

    Stop use and ask a doctor if

    • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

    Keep out of reach of children. 

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

    If pregnant or breast-feeding,

    ask a health professional before use

  • Directions:

    • Adults and children 2 years of age or older:  Apply to affected area not more than 3 to 4 times daily.
    • Children under 2 years of age:  consult a doctor.
  • Other information:

    • Store at 20-25°C (68-77°F) and protect from moisture.
  • Other Ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Benzoic Acid, Cannabis Sativus (Hemp) Seed Oil, Carbomer, Carrageenan, Ethylhexylglycerin, I-Arginine, PEG-8, Phenoxyethanol, Polysorbate-20, Propylene Glycol, Tocopherol Acetate (Vitamin E), Triethanolamine.

  • Questions?

    (800) 243-8370

  • Package Labeling:

    Jar

  • INGREDIENTS AND APPEARANCE
    SYREN INTIMATE PAIN RELIEF 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69233-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    HEMP (UNII: TD1MUT01Q7)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ARGININE (UNII: 94ZLA3W45F)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69233-122-021 in 1 BOX01/10/2020
    160 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/10/2020
    Labeler - Icon Health Science, LLC (079435759)
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