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Peter Island Continous sunscreen - 10056-709-34 - (OXYBENZONE, AVOBENZONE, OCTOCRYLENE)

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Drug Information of Peter Island Continous sunscreen

Product NDC: 10056-709
Proprietary Name: Peter Island Continous sunscreen
Non Proprietary Name: OXYBENZONE, AVOBENZONE, OCTOCRYLENE
Active Ingredient(s): 3; 5; 5    g/100g; g/100g; g/100g & nbsp;   OXYBENZONE, AVOBENZONE, OCTOCRYLENE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Peter Island Continous sunscreen

Product NDC: 10056-709
Labeler Name: Access Business Group LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130709

Package Information of Peter Island Continous sunscreen

Package NDC: 10056-709-34
Package Description: 177 g in 1 BOTTLE, PLASTIC (10056-709-34)

NDC Information of Peter Island Continous sunscreen

NDC Code 10056-709-34
Proprietary Name Peter Island Continous sunscreen
Package Description 177 g in 1 BOTTLE, PLASTIC (10056-709-34)
Product NDC 10056-709
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OXYBENZONE, AVOBENZONE, OCTOCRYLENE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20130709
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Access Business Group LLC
Substance Name AVOBENZONE; OCTISALATE; OXYBENZONE
Strength Number 3; 5; 5
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Peter Island Continous sunscreen


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