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FEIX
FEIX - 66854-024-01 - (SULFUR)
Drug Information of FEIX
| Product NDC: | 66854-024 |
| Proprietary Name: | FEIX |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | .5; .2 mL/100mL; mL/100mL & nbsp; SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FEIX
| Product NDC: | 66854-024 |
| Labeler Name: | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120630 |
Package Information of FEIX
| Package NDC: | 66854-024-01 |
| Package Description: | 280 mL in 1 BOTTLE (66854-024-01) |
NDC Information of FEIX
| NDC Code | 66854-024-01 |
| Proprietary Name | FEIX |
| Package Description | 280 mL in 1 BOTTLE (66854-024-01) |
| Product NDC | 66854-024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Substance Name | DIPYRITHIONE; SULFUR |
| Strength Number | .5; .2 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |
