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Herpetrol
Herpetrol - 52389-179-07 - (Benzalkonium chloride, menthol, petrolatum)
Drug Information of Herpetrol
| Product NDC: | 52389-179 |
| Proprietary Name: | Herpetrol |
| Non Proprietary Name: | Benzalkonium chloride, menthol, petrolatum |
| Active Ingredient(s): | 1.3; 10; 970 mg/g; mg/g; mg/g & nbsp; Benzalkonium chloride, menthol, petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Herpetrol
| Product NDC: | 52389-179 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050630 |
Package Information of Herpetrol
| Package NDC: | 52389-179-07 |
| Package Description: | 1 TUBE in 1 CARTON (52389-179-07) > 7 g in 1 TUBE (52389-179-01) |
NDC Information of Herpetrol
| NDC Code | 52389-179-07 |
| Proprietary Name | Herpetrol |
| Package Description | 1 TUBE in 1 CARTON (52389-179-07) > 7 g in 1 TUBE (52389-179-01) |
| Product NDC | 52389-179 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium chloride, menthol, petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20050630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE; MENTHOL; PETROLATUM |
| Strength Number | 1.3; 10; 970 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
