Label: PROLAYED LIDOCAINE MALE GENITAL DESENSITIZER- lidocaine ointment
- NDC Code(s): 71262-006-15
- Packager: ViaDerma Distribution, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 2, 2023
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INGREDIENTS AND APPEARANCE
PROLAYED LIDOCAINE MALE GENITAL DESENSITIZER
lidocaine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71262-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength SORBIC ACID (UNII: X045WJ989B) ACETIC ACID (UNII: Q40Q9N063P) ASCORBIC ACID (UNII: PQ6CK8PD0R) CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) CHOLECALCIFEROL (UNII: 1C6V77QF41) DIMETHYL SULFOXIDE (UNII: YOW8V9698H) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERIN (UNII: PDC6A3C0OX) HISTIDINE (UNII: 4QD397987E) MAGNESIUM STEARATE (UNII: 70097M6I30) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71262-006-15 1 in 1 BOX 06/23/2017 1 15 mL in 1 BOTTLE; 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 06/23/2017 Labeler - ViaDerma Distribution, Inc. (081113521)