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SPF 30 Sunscreen - 57817-300-38 - (OCTINOXATE OXYBENZONE Octisalate)

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Drug Information of SPF 30 Sunscreen

Product NDC: 57817-300
Proprietary Name: SPF 30 Sunscreen
Non Proprietary Name: OCTINOXATE OXYBENZONE Octisalate
Active Ingredient(s): 6; 5; 4    g/100g; g/100g; g/100g & nbsp;   OCTINOXATE OXYBENZONE Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SPF 30 Sunscreen

Product NDC: 57817-300
Labeler Name: Hangzhou Haorun Technology CO.,LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130418

Package Information of SPF 30 Sunscreen

Package NDC: 57817-300-38
Package Description: 40 g in 1 PACKAGE (57817-300-38)

NDC Information of SPF 30 Sunscreen

NDC Code 57817-300-38
Proprietary Name SPF 30 Sunscreen
Package Description 40 g in 1 PACKAGE (57817-300-38)
Product NDC 57817-300
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE OXYBENZONE Octisalate
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20130418
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Hangzhou Haorun Technology CO.,LTD.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 6; 5; 4
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of SPF 30 Sunscreen


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