Daily Fade - 59735-306-56 - (Sunscreen)

Alphabetical Index


Drug Information of Daily Fade

Product NDC: 59735-306
Proprietary Name: Daily Fade
Non Proprietary Name: Sunscreen
Active Ingredient(s): 2; 5    g/100g; g/100g & nbsp;   Sunscreen
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Daily Fade

Product NDC: 59735-306
Labeler Name: Biocosetic Research Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20060306

Package Information of Daily Fade

Package NDC: 59735-306-56
Package Description: 1 TUBE in 1 CARTON (59735-306-56) > 56 g in 1 TUBE

NDC Information of Daily Fade

NDC Code 59735-306-56
Proprietary Name Daily Fade
Package Description 1 TUBE in 1 CARTON (59735-306-56) > 56 g in 1 TUBE
Product NDC 59735-306
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sunscreen
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20060306
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Biocosetic Research Labs
Substance Name AVOBENZONE; OCTINOXATE
Strength Number 2; 5
Strength Unit g/100g; g/100g
Pharmaceutical Classes

Complete Information of Daily Fade


General Information