Product NDC: | 11822-3410 |
Proprietary Name: | RITE AID RENEWAL |
Non Proprietary Name: | ENSULIZOLE |
Active Ingredient(s): | 2; 7.5; 7.5; 1.9 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; ENSULIZOLE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-3410 |
Labeler Name: | RITE AID CORPORATION |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110721 |
Package NDC: | 11822-3410-2 |
Package Description: | 50 mL in 1 TUBE (11822-3410-2) |
NDC Code | 11822-3410-2 |
Proprietary Name | RITE AID RENEWAL |
Package Description | 50 mL in 1 TUBE (11822-3410-2) |
Product NDC | 11822-3410 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ENSULIZOLE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110721 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | RITE AID CORPORATION |
Substance Name | ENSULIZOLE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
Strength Number | 2; 7.5; 7.5; 1.9 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |