| Product NDC: | 11822-9014 |
| Proprietary Name: | Rite Aid Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 5; 6 g/100g; g/100g; g/100g & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-9014 |
| Labeler Name: | RITE AID CORPORATION |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121205 |
| Package NDC: | 11822-9014-9 |
| Package Description: | 453 g in 1 BOTTLE, PLASTIC (11822-9014-9) |
| NDC Code | 11822-9014-9 |
| Proprietary Name | Rite Aid Sunscreen |
| Package Description | 453 g in 1 BOTTLE, PLASTIC (11822-9014-9) |
| Product NDC | 11822-9014 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121205 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | RITE AID CORPORATION |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 5; 6 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |