Label: SKINS DELAY MAXIMUM STRENGTH LIDOCAINE- lidocaine hydrochloride solution

  • NDC Code(s): 81923-199-00
  • Packager: SKINS SEXUAL HEALTH LIMITED
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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

  • DRUG FACTS

  • Active Ingredient (per spray):

    Lidocaine HCL 10mg

    Purpose:

    Anaesthetic

  • USES:

    Helps to temporarily prevent premature ejaculation.

  • WARNINGS:

    • Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician.
    • For external use only.
    • Avoid contact with eyes. 
    • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician.

    Keep out of reach of children.

    • If product is swallowed, get medical attention or contact poison control center immediately.

    Do not use

    • on broken or inflamed skin, if partner is pregnant, on large areas of the body, or orally.
  • DIRECTIONS:

    Apply 3 or more sprays to the head and shaft of the penis depending on the level of anaesthesia desired. . Massage into the penis for around twenty seconds or until optimal absorption is reached. Wash hands thoroughly after use. You will feel the product start to work after 3-5 minutes so although you can apply up to 10 sprays we recommend waiting to feel the full effects before applying any more. You should always use minimum effective quantity. Do not exceed 10 sprays

  • Other Information:

    • Store in a cool dry place out of direct sunlight. Store below 30°c (86°F). 
    • Do  not use if seal under cap is broken or missing.
  • QUESTIONS?

    You can contact Skins on  +44 1636 593943

  • INACTIVE INGREDIENTS:

    Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), l-Arginine, Ascorbic Acid (Vitamin C), Chamomilla Recutita (Chamomile) Extract, Epimedium (Horny Goat) Weed Extract, Ethylhexylglycerin, Folic Acid (Vitamin B9), Ginko Biloba Extract, Glycerin, Glycyrrhiza Glabra (Licorice) Root Extract, Hydroxyethylcellulose, Hypericum Perforatum (St John’s) Extract, Lepidium Meyenii (Maca) Root Extract, Niacin, Panax Ginseng Root Extract, Parfum (Fragrance), Phenoxyethanol, Polysorbate 20, Serenoa Serrulata (Saw Palmetto) Extract, l-Carnitine, Tocopheryl Acetate (Vitamin E), Tribulus Terrestris Extract, Zemea (Corn) Propanediol.

  • Package Labeling:

    Label3

  • INGREDIENTS AND APPEARANCE
    SKINS DELAY MAXIMUM STRENGTH LIDOCAINE 
    lidocaine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81923-199
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARGININE (UNII: 94ZLA3W45F)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    CHAMOMILE (UNII: FGL3685T2X)  
    EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    FOLIC ACID (UNII: 935E97BOY8)  
    GINKGO (UNII: 19FUJ2C58T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)  
    LEPIDIUM MEYENII ROOT (UNII: HP7119212T)  
    NIACIN (UNII: 2679MF687A)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SAW PALMETTO (UNII: J7WWH9M8QS)  
    LEVOCARNITINE (UNII: 0G389FZZ9M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRIBULUS TERRESTRIS WHOLE (UNII: 4X4HLN92OT)  
    CORN (UNII: 0N8672707O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81923-199-001 in 1 BOX05/25/2021
    115 mL in 1 CYLINDER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/25/2021
    Labeler - SKINS SEXUAL HEALTH LIMITED (221947744)