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NATURALTECH PURIFYING ANTI-DANDRUFF
NATURALTECH PURIFYING ANTI-DANDRUFF - 64724-1017-1 - (PYRITHIONE ZINC)
Drug Information of NATURALTECH PURIFYING ANTI-DANDRUFF
| Product NDC: | 64724-1017 |
| Proprietary Name: | NATURALTECH PURIFYING ANTI-DANDRUFF |
| Non Proprietary Name: | PYRITHIONE ZINC |
| Active Ingredient(s): | .48 mL/100mL & nbsp; PYRITHIONE ZINC |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NATURALTECH PURIFYING ANTI-DANDRUFF
| Product NDC: | 64724-1017 |
| Labeler Name: | Davines S.p.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120229 |
Package Information of NATURALTECH PURIFYING ANTI-DANDRUFF
| Package NDC: | 64724-1017-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (64724-1017-1) > 150 mL in 1 BOTTLE |
NDC Information of NATURALTECH PURIFYING ANTI-DANDRUFF
| NDC Code | 64724-1017-1 |
| Proprietary Name | NATURALTECH PURIFYING ANTI-DANDRUFF |
| Package Description | 1 BOTTLE in 1 CARTON (64724-1017-1) > 150 mL in 1 BOTTLE |
| Product NDC | 64724-1017 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | PYRITHIONE ZINC |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120229 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Davines S.p.A. |
| Substance Name | PYRITHIONE ZINC |
| Strength Number | .48 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
