OLAY AGE DEFYING ADVANCED WITH HYALURONIC ACID HYDRATING MOISTURIZERPROTECTIVE RENEWAL BROAD SPECTRUM SPF 15- octinoxate and zinc oxide lotion

Olay Age Defying Advanced with Hyaluronic Acid Hydrating MoisturizerProtective Renewal by

Drug Labeling and Warnings

Olay Age Defying Advanced with Hyaluronic Acid Hydrating MoisturizerProtective Renewal by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients	Purpose
Octinoxate 6.0%	Sunscreen
Zinc Oxide 3.0%	Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 15 minutes before sun exposure
• reapply at least every 2 hours
• use water resistant sunscreen if swimming or sweating
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
• children under 6 months: ask a doctor

Other information

• protect this product from excessive heat and direct sun

Inactive ingredients

Water, glycerin, isohexadecane, sodium hyaluronate, aloe barbadensis leaf extract, tocopheryl acetate, steareth-21, cyclopentasiloxane, polyacrylamide, stearyl alcohol, C13-14 isoparaffin, behenyl alcohol, fragrance, ethylhexyl salicylate, cetyl alcohol, DMDM hydantoin, PEG/PPG-20/20 dimethicone, laureth-7, steareth-2, disodium EDTA, triethoxycaprylylsilane, oleth-3 phosphate, iodopropynyl butylcarbamate.

Questions or comments?

Call 1-800-285-5170

SPL UNCLASSIFIED SECTION

Dist. by
PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 120 mL Bottle Carton

OLAY

AGE DEFYING

ADVANCED

WITH HYALURONIC ACID

15

HYDRATING MOISTURIZER
with sunscreen

BROAD SPECTRUM SPF 15

100 mL (3.4 FL OZ)

INGREDIENTS AND APPEARANCE

OLAY AGE DEFYING ADVANCED WITH HYALURONIC ACID HYDRATING MOISTURIZERPROTECTIVE RENEWAL  BROAD SPECTRUM SPF 15
octinoxate and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-180
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K)
OCTISALATE (UNII: 4X49Y0596W)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ISOHEXADECANE (UNII: 918X1OUF1E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
STEARETH-21 (UNII: 53J3F32P58)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
DOCOSANOL (UNII: 9G1OE216XY)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
CETYL ALCOHOL (UNII: 936JST6JCN)
DMDM HYDANTOIN (UNII: BYR0546TOW)
STEARETH-2 (UNII: V56DFE46J5)
EDETATE DISODIUM (UNII: 7FLD91C86K)
LAURETH-7 (UNII: Z95S6G8201)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-180-10	1 in 1 CARTON	06/27/2017	05/24/2020
1		100 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	06/27/2017	05/24/2020

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Establishment
Name	Address	ID/FEI	Business Operations
The Procter & Gamble Manufacturing Company		017745779	manufacture(69423-180) , pack(69423-180)