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NO-AD 15 Sunscreen - 62802-212-16 - (avobenzone, homosalate,octisalate)

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Drug Information of NO-AD 15 Sunscreen

Product NDC: 62802-212
Proprietary Name: NO-AD 15 Sunscreen
Non Proprietary Name: avobenzone, homosalate,octisalate
Active Ingredient(s): 1.2; 7.5; 5    mL/100mL; mL/100mL; mL/100mL & nbsp;   avobenzone, homosalate,octisalate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of NO-AD 15 Sunscreen

Product NDC: 62802-212
Labeler Name: Sun & Skin Care Research, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120101

Package Information of NO-AD 15 Sunscreen

Package NDC: 62802-212-16
Package Description: 475 mL in 1 BOTTLE (62802-212-16)

NDC Information of NO-AD 15 Sunscreen

NDC Code 62802-212-16
Proprietary Name NO-AD 15 Sunscreen
Package Description 475 mL in 1 BOTTLE (62802-212-16)
Product NDC 62802-212
Product Type Name HUMAN OTC DRUG
Non Proprietary Name avobenzone, homosalate,octisalate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Sun & Skin Care Research, LLC
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE
Strength Number 1.2; 7.5; 5
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of NO-AD 15 Sunscreen


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