Label: 5 ELEMENTUM LIDOCAINE MALE GENITAL DESENSITIZER- lidocaine male genital desensitizer spray
- NDC Code(s): 87203-002-01, 87203-002-02
- Packager: MSVENTURESGROUP OÜ
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 8, 2026
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- Official Label (Printer Friendly)
- PURPOSE
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INDICATIONS & USAGE
Gently shake bottle. Hold upright and press pump until spray dispenses.
• Apply 3 or more sprays, not to exceed 10, to head and shaft of penis 10 minutes before sexual intercourse or use as directed by a doctor.
• Wash product off after intercourse.
• for temporary male genital desensitization, helping to slow the onset of ejaculation
• helps in temporarily prolonging the time until ejaculation
• for reducing oversensitivity in the male in advance of intercourse - WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
5 ELEMENTUM LIDOCAINE MALE GENITAL DESENSITIZER
lidocaine male genital desensitizer sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:87203-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 1 g in 10 g Inactive Ingredients Ingredient Name Strength METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DIPROPYLENE GLYCOL (UNII: E107L85C40) CAPRYLYL GLYCOL (UNII: 00YIU5438U) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:87203-002-01 1 in 1 BOX 05/08/2026 1 10 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 2 NDC:87203-002-02 2 in 1 BOX 05/08/2026 2 10 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/08/2026 Labeler - MSVENTURESGROUP OÜ (536418682) Registrant - MSVENTURESGROUP OÜ (536418682) Establishment Name Address ID/FEI Business Operations Zhejiang Shini Nursing Products Technology Co., Ltd. 713979927 manufacture(87203-002)

