| Product NDC: | 11822-6181 |
| Proprietary Name: | RITE AID RENEWAL |
| Non Proprietary Name: | SELENIUM SULFIDE |
| Active Ingredient(s): | 10 mg/mL & nbsp; SELENIUM SULFIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-6181 |
| Labeler Name: | RITE AID CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130326 |
| Package NDC: | 11822-6181-4 |
| Package Description: | 420 mL in 1 BOTTLE, PLASTIC (11822-6181-4) |
| NDC Code | 11822-6181-4 |
| Proprietary Name | RITE AID RENEWAL |
| Package Description | 420 mL in 1 BOTTLE, PLASTIC (11822-6181-4) |
| Product NDC | 11822-6181 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SELENIUM SULFIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130326 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | RITE AID CORPORATION |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |