Home > National Drug Code (NDC) > NO-AD Splash 30 Sunscreen

NO-AD Splash 30 Sunscreen - 62802-213-16 - (avobenzone, homosalate, octisalate, oxybenzone)

Alphabetical Index


Drug Information of NO-AD Splash 30 Sunscreen

Product NDC: 62802-213
Proprietary Name: NO-AD Splash 30 Sunscreen
Non Proprietary Name: avobenzone, homosalate, octisalate, oxybenzone
Active Ingredient(s): 2; 10; 5; 3    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   avobenzone, homosalate, octisalate, oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of NO-AD Splash 30 Sunscreen

Product NDC: 62802-213
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 Splash 30 Sunscreen

Package NDC: 62802-213-16
Package Description: 475 mL in 1 BOTTLE (62802-213-16)

NDC Information of NO-AD Splash 30 Sunscreen

NDC Code 62802-213-16
Proprietary Name NO-AD Splash 30 Sunscreen
Package Description 475 mL in 1 BOTTLE (62802-213-16)
Product NDC 62802-213
Product Type Name HUMAN OTC DRUG
Non Proprietary Name avobenzone, homosalate, octisalate, oxybenzone
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; OXYBENZONE
Strength Number 2; 10; 5; 3
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of NO-AD Splash 30 Sunscreen


General Information