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SunScreen SPF30 - 31190-500-60 - (OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE)

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Drug Information of SunScreen SPF30

Product NDC: 31190-500
Proprietary Name: SunScreen SPF30
Non Proprietary Name: OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
Active Ingredient(s): 7.5; 2; 4; 2.5    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of SunScreen SPF30

Product NDC: 31190-500
Labeler Name: Shanghai Kejing Cleaning Products Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100422

Package Information of SunScreen SPF30

Package NDC: 31190-500-60
Package Description: 1 BOTTLE in 1 CARTON (31190-500-60) > 60 mL in 1 BOTTLE

NDC Information of SunScreen SPF30

NDC Code 31190-500-60
Proprietary Name SunScreen SPF30
Package Description 1 BOTTLE in 1 CARTON (31190-500-60) > 60 mL in 1 BOTTLE
Product NDC 31190-500
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100422
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Shanghai Kejing Cleaning Products Co., Ltd.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
Strength Number 7.5; 2; 4; 2.5
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of SunScreen SPF30


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