Home > National Drug Code (NDC) > All Day Sunscreen with SPF 30

All Day Sunscreen with SPF 30 - 68572-6005-4 - (Oxybenzone, Octinoxate, Octisalate, and Homosalate)

Alphabetical Index


Drug Information of All Day Sunscreen with SPF 30

Product NDC: 68572-6005
Proprietary Name: All Day Sunscreen with SPF 30
Non Proprietary Name: Oxybenzone, Octinoxate, Octisalate, and Homosalate
Active Ingredient(s): 5.9; 8.9; 5.9; 8.9    g/118mL; g/118mL; g/118mL; g/118mL & nbsp;   Oxybenzone, Octinoxate, Octisalate, and Homosalate
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of All Day Sunscreen with SPF 30

Product NDC: 68572-6005
Labeler Name: Kara Vita, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040101

Package Information of All Day Sunscreen with SPF 30

Package NDC: 68572-6005-4
Package Description: 1 BOTTLE in 1 CARTON (68572-6005-4) > 59 mL in 1 BOTTLE

NDC Information of All Day Sunscreen with SPF 30

NDC Code 68572-6005-4
Proprietary Name All Day Sunscreen with SPF 30
Package Description 1 BOTTLE in 1 CARTON (68572-6005-4) > 59 mL in 1 BOTTLE
Product NDC 68572-6005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Oxybenzone, Octinoxate, Octisalate, and Homosalate
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20040101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kara Vita, Inc.
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 5.9; 8.9; 5.9; 8.9
Strength Unit g/118mL; g/118mL; g/118mL; g/118mL
Pharmaceutical Classes

Complete Information of All Day Sunscreen with SPF 30


General Information