NDC | 13537-261-61, 13537-261-62, 13537-261-63, 13537-261-64, 13537-261-65 |
Set ID | fcd21129-4cb4-4cfb-9865-3cfde69eac0b |
Category | HUMAN OTC DRUG LABEL |
Packager | Ventura Corporation, LTDA |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- WARNINGS
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL - 50 g jar
-
INGREDIENTS AND APPEARANCE
SUPREMACIE NX JOUR
ensulizole, homosalate, octinoxate, and oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13537-261 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Ensulizole (UNII: 9YQ9DI1W42) (Ensulizole - UNII:9YQ9DI1W42) Ensulizole 0.001 g in 5 g Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate 0.001 g in 5 g Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 0.00375 g in 5 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 0.002 g in 5 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13537-261-64 1 in 1 BOX 1 NDC:13537-261-61 5 g in 1 TUBE 2 NDC:13537-261-65 1 in 1 JAR 2 NDC:13537-261-62 50 g in 1 JAR 3 NDC:13537-261-63 1 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part352 02/19/2010 Labeler - Ventura Corporation, LTDA (602751344)