Home > National Drug Code (NDC) > Radiant C UVA/UVB Sunscreen

Radiant C UVA/UVB Sunscreen - 51785-445-01 - (Avobenzone, Octinoxate, and Oxybenzone)

Alphabetical Index


Drug Information of Radiant C UVA/UVB Sunscreen

Product NDC: 51785-445
Proprietary Name: Radiant C UVA/UVB Sunscreen
Non Proprietary Name: Avobenzone, Octinoxate, and Oxybenzone
Active Ingredient(s): .03; .07; .004    g/mL; g/mL; g/mL & nbsp;   Avobenzone, Octinoxate, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Radiant C UVA/UVB Sunscreen

Product NDC: 51785-445
Labeler Name: Herbalife International of America
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130401

Package Information of Radiant C UVA/UVB Sunscreen

Package NDC: 51785-445-01
Package Description: 200 mL in 1 TUBE (51785-445-01)

NDC Information of Radiant C UVA/UVB Sunscreen

NDC Code 51785-445-01
Proprietary Name Radiant C UVA/UVB Sunscreen
Package Description 200 mL in 1 TUBE (51785-445-01)
Product NDC 51785-445
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Octinoxate, and Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Herbalife International of America
Substance Name AVOBENZONE; OCTINOXATE; OXYBENZONE
Strength Number .03; .07; .004
Strength Unit g/mL; g/mL; g/mL
Pharmaceutical Classes

Complete Information of Radiant C UVA/UVB Sunscreen


General Information