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ProClearz
ProClearz - 29784-181-02 - (Tolnaftate)
Drug Information of ProClearz
| Product NDC: | 29784-181 |
| Proprietary Name: | ProClearz |
| Non Proprietary Name: | Tolnaftate |
| Active Ingredient(s): | 10 mg/mL & nbsp; Tolnaftate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ProClearz
| Product NDC: | 29784-181 |
| Labeler Name: | Profoot, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121022 |
Package Information of ProClearz
| Package NDC: | 29784-181-02 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BOX (29784-181-02) > 30 mL in 1 BOTTLE, WITH APPLICATOR (29784-181-01) |
NDC Information of ProClearz
| NDC Code | 29784-181-02 |
| Proprietary Name | ProClearz |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (29784-181-02) > 30 mL in 1 BOTTLE, WITH APPLICATOR (29784-181-01) |
| Product NDC | 29784-181 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121022 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Profoot, Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
