NDC Code(s) : 10812-702-01
Packager : Johnson & Johnson Consumer Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Neutrogena Wet Skin Swim Humidity Sweat Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone AEROSOL, SPRAY
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10812-702
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Avobenzone(UNII: G63QQF2NOX)
(Avobenzone - UNII:G63QQF2NOX) 		Avobenzone30 mg in 1 g
Homosalate(UNII: V06SV4M95S)
(Homosalate - UNII:V06SV4M95S) 		Homosalate150 mg in 1 g
Octisalate(UNII: 4X49Y0596W)
(Octisalate - UNII:4X49Y0596W) 		Octisalate50 mg in 1 g
Octocrylene(UNII: 5A68WGF6WM)
(Octocrylene - UNII:5A68WGF6WM) 		Octocrylene100 mg in 1 g
Oxybenzone(UNII: 95OOS7VE0Y)
(Oxybenzone - UNII:95OOS7VE0Y) 		Oxybenzone60 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
Ascorbyl Palmitate(UNII: QN83US2B0N)
Butyloctyl Salicylate(UNII: 2EH13UN8D3)
Diethylhexyl 2,6-Naphthalate(UNII: I0DQJ7YGXM)
Dimethicone(UNII: 92RU3N3Y1O)
Dimethyl Ether(UNII: AM13FS69BX)
Nelumbo Nucifera Flower Wax(UNII: U01S6C427I)
Vitamin A Palmitate(UNII: 1D1K0N0VVC)
.Alpha.-Tocopherol Acetate(UNII: 9E8X80D2L0)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:10812-702-01141 g in 1 CAN Type 0: Not a Combination Product16/10/2010
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part352 10/16/2010 10/01/2018

PRINCIPAL DISPLAY PANEL

BREAKTHROUGH AWARD
allure
THE BEAUTY EXPERT
2011

Neutrogena®

wet skin

SWIM•HUMIDITY•SWEAT

SUNSCREEN

Broad
Spectrum
SPF 85+

helioplex®
broad spectrum uva•uvb

full strength protection
on wet or dry skin
water resistant (80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

NET WT 5.0 OZ (141 g)

Principal Display Panel - 141 g Can Label