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Correway Sunscreen (Non-waterproof)
Correway Sunscreen (Non-waterproof) - 50600-004-01 - (Octinoxate)
Drug Information of Correway Sunscreen (Non-waterproof)
| Product NDC: | 50600-004 |
| Proprietary Name: | Correway Sunscreen (Non-waterproof) |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 35; 75; 50; 35 mg/g; mg/g; mg/g; mg/g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Correway Sunscreen (Non-waterproof)
| Product NDC: | 50600-004 |
| Labeler Name: | Ningbo Correway Cosmetics Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100720 |
Package Information of Correway Sunscreen (Non-waterproof)
| Package NDC: | 50600-004-01 |
| Package Description: | 42.6 g in 1 TUBE (50600-004-01) |
NDC Information of Correway Sunscreen (Non-waterproof)
| NDC Code | 50600-004-01 |
| Proprietary Name | Correway Sunscreen (Non-waterproof) |
| Package Description | 42.6 g in 1 TUBE (50600-004-01) |
| Product NDC | 50600-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100720 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ningbo Correway Cosmetics Co., Ltd. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 35; 75; 50; 35 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
