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HEB Dandruff
HEB Dandruff - 37808-613-14 - (Selenium Sulfide)
Drug Information of HEB Dandruff
| Product NDC: | 37808-613 |
| Proprietary Name: | HEB Dandruff |
| Non Proprietary Name: | Selenium Sulfide |
| Active Ingredient(s): | 1 mL/100mL & nbsp; Selenium Sulfide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HEB Dandruff
| Product NDC: | 37808-613 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110808 |
Package Information of HEB Dandruff
| Package NDC: | 37808-613-14 |
| Package Description: | 420 mL in 1 BOTTLE, PLASTIC (37808-613-14) |
NDC Information of HEB Dandruff
| NDC Code | 37808-613-14 |
| Proprietary Name | HEB Dandruff |
| Package Description | 420 mL in 1 BOTTLE, PLASTIC (37808-613-14) |
| Product NDC | 37808-613 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Selenium Sulfide |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20110808 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
