Home > National Drug Code (NDC) > SUNZONE FAMILY SPF 60

SUNZONE FAMILY SPF 60 - 50021-062-01 - (Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.)

Alphabetical Index


Drug Information of SUNZONE FAMILY SPF 60

Product NDC: 50021-062
Proprietary Name: SUNZONE FAMILY SPF 60
Non Proprietary Name: Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.
Active Ingredient(s): 4.65; 18.6; 7.75; 7.75; 7.75; 9.3    g/155g; g/155g; g/155g; g/155g; g/155g; g/155g & nbsp;   Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of SUNZONE FAMILY SPF 60

Product NDC: 50021-062
Labeler Name: Empack Spraytech Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121116

Package Information of SUNZONE FAMILY SPF 60

Package NDC: 50021-062-01
Package Description: 155 g in 1 CAN (50021-062-01)

NDC Information of SUNZONE FAMILY SPF 60

NDC Code 50021-062-01
Proprietary Name SUNZONE FAMILY SPF 60
Package Description 155 g in 1 CAN (50021-062-01)
Product NDC 50021-062
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate.
Dosage Form Name AEROSOL, SPRAY
Route Name TOPICAL
Start Marketing Date 20121116
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Empack Spraytech Inc.
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 4.65; 18.6; 7.75; 7.75; 7.75; 9.3
Strength Unit g/155g; g/155g; g/155g; g/155g; g/155g; g/155g
Pharmaceutical Classes

Complete Information of SUNZONE FAMILY SPF 60


General Information