Label: STAMA PRO- lidocaine spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70107-302-09 - Packager: Cerno Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 11, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- Stop use and ask a doctor:
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DOSAGE & ADMINISTRATION
Remove the protective cap. Press the actuator down repeatedly until product dispenses to prime spray pump.
Apply 3 or more sprays, not to exceed 10, to head and shaft of penis 8 minutes before intercourse, or use as directed by a
doctor. Wash product off after intercourse. After spraying, place the cap back on. - PURPOSE
- Other Information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STAMA PRO
lidocaine sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70107-302 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 96 mg in 1 mL Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70107-302-09 13.5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/11/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 01/11/2017 Labeler - Cerno Pharmaceuticals (079821037) Establishment Name Address ID/FEI Business Operations Cerno Pharmaceuticals 079821037 MANUFACTURE(70107-302)