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Pure Foam
Pure Foam - 50452-773-26 - (ALCOHOL)
Drug Information of Pure Foam
| Product NDC: | 50452-773 |
| Proprietary Name: | Pure Foam |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | 620 mg/g & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pure Foam
| Product NDC: | 50452-773 |
| Labeler Name: | Phoenix Research Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100131 |
Package Information of Pure Foam
| Package NDC: | 50452-773-26 |
| Package Description: | 454 g in 1 CAN (50452-773-26) |
NDC Information of Pure Foam
| NDC Code | 50452-773-26 |
| Proprietary Name | Pure Foam |
| Package Description | 454 g in 1 CAN (50452-773-26) |
| Product NDC | 50452-773 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100131 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Phoenix Research Industries, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 620 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
