NDC Code(s) : 37000-234-12
Packager : Procter & Gamble Manufacturing Company

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Olay Age Defying Mature Skin Octinoxate and Zinc Oxide LOTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:37000-234
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Octinoxate(UNII: 4Y5P7MUD51)
(Octinoxate - UNII:4Y5P7MUD51) 		Octinoxate6 g in 100 mL
Zinc Oxide(UNII: SOI2LOH54Z)
(Zinc Oxide - UNII:SOI2LOH54Z) 		Zinc Oxide3 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
water(UNII: 059QF0KO0R)
glycerin(UNII: PDC6A3C0OX)
isohexadecane(UNII: 918X1OUF1E)
C13-14 isoparaffin(UNII: E4F12ROE70)
laureth-7(UNII: Z95S6G8201)
cyclomethicone 5(UNII: 0THT5PCI0R)
PEG/PPG-20/20 dimethicone(UNII: BA94B7CK8K)
triethoxycaprylylsilane(UNII: LDC331P08E)
steareth-21(UNII: 53J3F32P58)
stearyl alcohol(UNII: 2KR89I4H1Y)
docosanol(UNII: 9G1OE216XY)
cetyl alcohol(UNII: 936JST6JCN)
DMDM hydantoin(UNII: BYR0546TOW)
iodopropynyl butylcarbamate(UNII: 603P14DHEB)
octisalate(UNII: 4X49Y0596W)
.alpha.-tocopherol acetate(UNII: 9E8X80D2L0)
ascorbic acid(UNII: PQ6CK8PD0R)
edetate disodium(UNII: 7FLD91C86K)
steareth-2(UNII: V56DFE46J5)
oleth-3 phosphate(UNII: 8Q0Z18J1VL)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:37000-234-121 in 1 CARTON 01/06/2012
1120 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part352 06/01/2012 04/11/2018

PRINCIPAL DISPLAY PANEL

OLAY ®
AGE DEFYING

CLASSIC

protective renewal lotion
with sunscreen
BROAD SPECTRUM SPF 15

4.0 FL OZ (120 mL)
15

Principal Display Panel