Label: POWERECT LIDOCAINE MALE DELAY- lidocaine hydrochloride solution
- NDC Code(s): 81923-366-00
- Packager: SKINS SEXUAL HEALTH LIMITED
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 6, 2023
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- DRUG FACTS
- ACTIVE INGREDIENT (per spray):
- USES:
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WARNINGS:
Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, • If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician. discontinue use and consult a physician.FOR EXTERNAL USE ONLY.Avoid contact with eyes.
- DIRECTIONS:
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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, Phenoxyethanol, Polysorbate 20, Serenoa Serrulata (Saw Palmetto) Extract, l-Carnitine, Tocopheryl Acetate (Vitamin E), Tribulus Terrestris Extract, Zemea (Corn) Propanediol.
- Other Information:
- QUESTIONS?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
POWERECT LIDOCAINE MALE DELAY
lidocaine hydrochloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81923-366 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGININE (UNII: 94ZLA3W45F) ASCORBIC ACID (UNII: PQ6CK8PD0R) CHAMOMILE (UNII: FGL3685T2X) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) FOLIC ACID (UNII: 935E97BOY8) 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:81923-366-00 15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 10/03/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/03/2022 Labeler - SKINS SEXUAL HEALTH LIMITED (221947744)
