NDC Code(s) : 69842-778-05
Packager : CVS

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Sunscreen SPF 50Avobenzone 3.0% Homosalate 15.0% Octisalate 5.0% Octocrylene 10.0% SPRAY
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69842-778
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Avobenzone(UNII: G63QQF2NOX)
(AVOBENZONE - UNII:G63QQF2NOX) 		Avobenzone3.0 1 in 100 mL
Homosalate(UNII: V06SV4M95S)
(HOMOSALATE - UNII:V06SV4M95S) 		Homosalate15.0 1 in 100 mL
Octisalate(UNII: 4X49Y0596W)
(OCTISALATE - UNII:4X49Y0596W) 		Octisalate5.0 1 in 100 mL
Octocrylene(UNII: 5A68WGF6WM)
(OCTOCRYLENE - UNII:5A68WGF6WM) 		Octocrylene10.0 1 in 100 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL(UNII: 3K9958V90M)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
Diethylhexyl Syringylidenemalonate(UNII: 3V5U97P248)
Glycerin(UNII: PDC6A3C0OX)
Stearoxytrimethylsilane(UNII: 9862TW94B2)
Tocopherol(UNII: R0ZB2556P8)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:69842-778-05177 mL in 1 BOTTLE Type 0: Not a Combination Product15/03/2016
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 03/15/2016

PRINCIPAL DISPLAY PANEL

image description