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 |