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Surfers Skin Sunscreen - 75916-4019-1 - (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE)

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Drug Information of Surfers Skin Sunscreen

Product NDC: 75916-4019
Proprietary Name: Surfers Skin Sunscreen
Non Proprietary Name: OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
Active Ingredient(s): 7.5; 3.45; 1; 1.95    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Surfers Skin Sunscreen

Product NDC: 75916-4019
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 Surfers Skin Sunscreen

Package NDC: 75916-4019-1
Package Description: 1 TUBE in 1 BOX (75916-4019-1) > 40 mL in 1 TUBE

NDC Information of Surfers Skin Sunscreen

NDC Code 75916-4019-1
Proprietary Name Surfers Skin Sunscreen
Package Description 1 TUBE in 1 BOX (75916-4019-1) > 40 mL in 1 TUBE
Product NDC 75916-4019
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 7.5; 3.45; 1; 1.95
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Surfers Skin Sunscreen


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