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Medicated Dandruff
Medicated Dandruff - 30142-246-39 - (Selenium sulfide)
Drug Information of Medicated Dandruff
| Product NDC: | 30142-246 |
| Proprietary Name: | Medicated Dandruff |
| Non Proprietary Name: | Selenium sulfide |
| Active Ingredient(s): | 1 kg/100L & nbsp; Selenium sulfide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Medicated Dandruff
| Product NDC: | 30142-246 |
| Labeler Name: | KROGER Co |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19900115 |
Package Information of Medicated Dandruff
| Package NDC: | 30142-246-39 |
| Package Description: | .325 L in 1 BOTTLE, PLASTIC (30142-246-39) |
NDC Information of Medicated Dandruff
| NDC Code | 30142-246-39 |
| Proprietary Name | Medicated Dandruff |
| Package Description | .325 L in 1 BOTTLE, PLASTIC (30142-246-39) |
| Product NDC | 30142-246 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Selenium sulfide |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 19900115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KROGER Co |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 1 |
| Strength Unit | kg/100L |
| Pharmaceutical Classes |
