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Correway Sunscreen (Non-waterproof) - 50600-004-01 - (Octinoxate)

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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

Complete Information of Correway Sunscreen (Non-waterproof)


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