Label: POPSTAR- delay spray spray

  • NDC Code(s): 85035-111-11, 85035-111-12
  • Packager: Pineapple Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2025

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  • Active Ingredient(s)

    Lidocaine 10mg .. Male Genital Desensitizer

  • Purpose

    Male Genital Desensitizer

  • Use

    Helps in temporarily slowing the onset of ejaculation.

  • Warnings

    For external use only.

    Do not use if you or your partner are allergic to lidocaine or topical anesthetics.

    When using this product

    Avoid contact with the eyes
    Do not spray on broken, irritated, or sensitive skin.

    Stop and ask a doctor if

    This product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision.
    You or your partner develop a rash or irritation, such as burning or itching.

    Ask a doctor or pharmacist before use

    If you have liver problems
    If your partner is, or may be pregnant.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of childern

    If swallowed, get medical attention or contact a Poison Control Center immediately.

  • Directions

    Gently shake bottle. Hold upright and press the pump until the spray dispenses. Apply 3 or more sprays, not to exceed 10, to head and shaft of penis 10 minutes betore intercourse or as directed by a doctor. Wash the product off after intercourse.

  • Other information

    Remove safety tab before use.
    Store at 68°-77° F (20-25° C).

  • Inactive ingredients

    Inactive Ingredients

    Purified Water, Propanediol, Alcohol, Aloe Barbadensis Leaf Juice, Laureth 9, PEG 8, Panthenol, Panax Ginseng Root Extract, Hydroxyethylcellulose, Menthyl Lactate, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Caprylyl Glycol, Phenoxyethanol,

    Ethylhexylglycerin

  • Package Label - Principal Display Panel

    Popstarlabel

  • INGREDIENTS AND APPEARANCE
    POPSTAR 
    delay spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85035-111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS10 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MENTHYL LACTATE (UNII: 2BF9E65L7I)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    LAURETH-9 (UNII: 0AWH8BFG9A)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PANAX GINSENG ROOT (UNII: CUQ3A77YXI)  
    PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PEG-8 (UNII: B697894SGQ)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85035-111-1275 in 1 BOX01/01/2025
    114.7 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    2NDC:85035-111-1114.7 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2025
    Labeler - Pineapple Brands LLC (119106097)
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