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Vagisil Anti Itch Maximum Strength
Vagisil Anti Itch Maximum Strength - 11509-0372-1 - (Benzocaine and Resorcinol)
Drug Information of Vagisil Anti Itch Maximum Strength
| Product NDC: | 11509-0372 |
| Proprietary Name: | Vagisil Anti Itch Maximum Strength |
| Non Proprietary Name: | Benzocaine and Resorcinol |
| Active Ingredient(s): | 200; 30 mg/g; mg/g & nbsp; Benzocaine and Resorcinol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vagisil Anti Itch Maximum Strength
| Product NDC: | 11509-0372 |
| Labeler Name: | Combe Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19740801 |
Package Information of Vagisil Anti Itch Maximum Strength
| Package NDC: | 11509-0372-1 |
| Package Description: | 1 TUBE in 1 CARTON (11509-0372-1) > 28 g in 1 TUBE |
NDC Information of Vagisil Anti Itch Maximum Strength
| NDC Code | 11509-0372-1 |
| Proprietary Name | Vagisil Anti Itch Maximum Strength |
| Package Description | 1 TUBE in 1 CARTON (11509-0372-1) > 28 g in 1 TUBE |
| Product NDC | 11509-0372 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine and Resorcinol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19740801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Combe Incorporated |
| Substance Name | BENZOCAINE; RESORCINOL |
| Strength Number | 200; 30 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
