Product NDC: | 75956-145 |
Proprietary Name: | Male Desensitizer |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | 3 g/100mL & nbsp; Benzocaine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75956-145 |
Labeler Name: | Kama Sutra |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110214 |
Package NDC: | 75956-145-02 |
Package Description: | 1 TUBE in 1 BOX (75956-145-02) > 50 mL in 1 TUBE (75956-145-01) |
NDC Code | 75956-145-02 |
Proprietary Name | Male Desensitizer |
Package Description | 1 TUBE in 1 BOX (75956-145-02) > 50 mL in 1 TUBE (75956-145-01) |
Product NDC | 75956-145 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110214 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kama Sutra |
Substance Name | BENZOCAINE |
Strength Number | 3 |
Strength Unit | g/100mL |
Pharmaceutical Classes |