| Product NDC: | 50600-003 |
| Proprietary Name: | Correway Sunscreen (Waterproof) |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 10; 35; 70; 80 mg/g; mg/g; mg/g; mg/g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50600-003 |
| 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: | 20100423 |
| Package NDC: | 50600-003-01 |
| Package Description: | 42.6 g in 1 TUBE (50600-003-01) |
| NDC Code | 50600-003-01 |
| Proprietary Name | Correway Sunscreen (Waterproof) |
| Package Description | 42.6 g in 1 TUBE (50600-003-01) |
| Product NDC | 50600-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100423 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ningbo Correway Cosmetics Co., Ltd. |
| Substance Name | AVOBENZONE; ENZACAMENE; OCTINOXATE; ZINC OXIDE |
| Strength Number | 10; 35; 70; 80 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |