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Pure Gel
Pure Gel - 50452-221-17 - (ALCOHOL)
Drug Information of Pure Gel
| Product NDC: | 50452-221 |
| Proprietary Name: | Pure Gel |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pure Gel
| Product NDC: | 50452-221 |
| Labeler Name: | Phoenix Research Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
Package Information of Pure Gel
| Package NDC: | 50452-221-17 |
| Package Description: | 532 mL in 1 BOTTLE, PLASTIC (50452-221-17) |
NDC Information of Pure Gel
| NDC Code | 50452-221-17 |
| Proprietary Name | Pure Gel |
| Package Description | 532 mL in 1 BOTTLE, PLASTIC (50452-221-17) |
| Product NDC | 50452-221 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Phoenix Research Industries, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
