NDC Code(s) : 60232-2585-4
Packager : Swiss American Products, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Elta MD UV SPF46 zinc oxide and octinoxate sunscreen SPRAY
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:60232-2585
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
zinc oxide(UNII: SOI2LOH54Z)
(zinc oxide - UNII:SOI2LOH54Z) 		zinc oxide93 g in 1000 g
octinoxate(UNII: 4Y5P7MUD51)
(octinoxate - UNII:4Y5P7MUD51) 		octinoxate75 g in 1000 g
Inactive Ingredients
Ingredient Name Strength
butylene glycol(UNII: 3XUS85K0RA)
phenoxyethanol(UNII: HIE492ZZ3T)
capryloyl glycine(UNII: 8TY5YO42NJ)
undecylenoyl glycine(UNII: 4D20464K2J)
CYCLOMETHICONE 5(UNII: 0THT5PCI0R)
water(UNII: 059QF0KO0R)
sodium chloride(UNII: 451W47IQ8X)
triethoxycaprylylsilane(UNII: LDC331P08E)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:60232-2585-44 g in 1 BOTTLE, SPRAY
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 06/01/2010

PRINCIPAL DISPLAY PANEL

image of chipboard box