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Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen - 75916-4020-5 - (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE)

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Drug Information of Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen

Product NDC: 75916-4020
Proprietary Name: Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen
Non Proprietary Name: OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
Active Ingredient(s): 75; 34.5; 10; 19.5    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen

Product NDC: 75916-4020
Labeler Name: Skin Alive, Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110131

Package Information of Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen

Package NDC: 75916-4020-5
Package Description: 2000 mL in 1 BOTTLE (75916-4020-5)

NDC Information of Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen

NDC Code 75916-4020-5
Proprietary Name Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen
Package Description 2000 mL in 1 BOTTLE (75916-4020-5)
Product NDC 75916-4020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110131
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Skin Alive, Ltd.
Substance Name OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 75; 34.5; 10; 19.5
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen


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