Label: HERBASOUL MALE GENITAL DESENSITIZER CREAM- benzocaine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 50664-100-36 - Packager: Bodon Med Laboratories Ltd.
- 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 February 23, 2010
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HERBASOUL MALE GENITAL DESENSITIZER CREAM
benzocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50664-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 4.5 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) MINERAL OIL (UNII: T5L8T28FGP) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50664-100-36 5 in 1 CARTON 1 1 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 02/23/2010 Labeler - Bodon Med Laboratories Ltd. (557643207) Registrant - Bodon Med Laboratories Ltd. (557643207) Establishment Name Address ID/FEI Business Operations Bodon Med Laboratories Ltd. 557643207 manufacture