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Peter Island Sunscreen - 10056-700-13 - (OCTOCRYLENE OXYBENZONE ZINC OXIDE)

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Drug Information of Peter Island Sunscreen

Product NDC: 10056-700
Proprietary Name: Peter Island Sunscreen
Non Proprietary Name: OCTOCRYLENE OXYBENZONE ZINC OXIDE
Active Ingredient(s): 5; 2; 3.9    g/100g; g/100g; g/100g & nbsp;   OCTOCRYLENE OXYBENZONE ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Peter Island Sunscreen

Product NDC: 10056-700
Labeler Name: ACCESS BUSINESS GROUP INTERNATIONAL LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121120

Package Information of Peter Island Sunscreen

Package NDC: 10056-700-13
Package Description: 113 g in 1 BOTTLE, PLASTIC (10056-700-13)

NDC Information of Peter Island Sunscreen

NDC Code 10056-700-13
Proprietary Name Peter Island Sunscreen
Package Description 113 g in 1 BOTTLE, PLASTIC (10056-700-13)
Product NDC 10056-700
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTOCRYLENE OXYBENZONE ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20121120
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name ACCESS BUSINESS GROUP INTERNATIONAL LLC
Substance Name OCTOCRYLENE; OXYBENZONE; ZINC OXIDE
Strength Number 5; 2; 3.9
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Peter Island Sunscreen


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