OLAY TOTAL EFFECTS ANTI-AGING MOISTURIZER BROAD SPECTRUM SPF 15 FRAGRANCE FREE- avobenzone, homosalate, octisalate, and octocrylene lotion

Olay Total Effects Anti-Aging Moisturizer by

Drug Labeling and Warnings

Olay Total Effects Anti-Aging Moisturizer 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

Avobenzone 3.0% Sunscreen

Homosalate 4.0% Sunscreen

Octisalate 4.5% Sunscreen

Octocrylene 2.6% 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, niacinamide 1, dimethicone, isopropyl isostearate, panthenol 2, tocopheryl acetate 3, camellia sinensis leaf extract, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, benzyl alcohol, PTFE, titanium dioxide, stearyl alcohol, behenyl alcohol, cetyl alcohol, methylparaben, dimethiconol, PEG-100 stearate, ethylparaben, carbomer, propylparaben, sodium ascorbyl phosphate, cetearyl glucoside, cetearyl alcohol, sodium hydroxide, BHT, disodium EDTA, stearic acid, palmitic acid, zinc oxide, iodopropynyl butylcarbamate, triethoxycaprylylsilane.

1

2

3

Active ingredients	Purpose
Avobenzone 3.0%	Sunscreen
Homosalate 4.0%	Sunscreen
Octisalate 4.5%	Sunscreen
Octocrylene 2.6%	Sunscreen

Questions or comments?

Call 1-800-285-5170

SPL UNCLASSIFIED SECTION

Distr. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton

OLAY

7 SKIN

BENEFITS

IN ONE

OLAY

TOTAL EFFECTS

7

IN

ONE

ANTI-AGING

MOISTURIZER WITH sunscreen

BROAD SPECTRUM SPF 15
FRAGRANCE-FREE

1.7 FL OZ (50 mL)

TEAAM

INGREDIENTS AND APPEARANCE

OLAY TOTAL EFFECTS ANTI-AGING MOISTURIZER BROAD SPECTRUM SPF 15 FRAGRANCE FREE
avobenzone, homosalate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-352
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	4 g in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.6 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
PALMITIC ACID (UNII: 2V16EO95H1)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
PANTHENOL (UNII: WV9CM0O67Z)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
DOCOSANOL (UNII: 9G1OE216XY)
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
PEG-100 STEARATE (UNII: YD01N1999R)
ETHYLPARABEN (UNII: 14255EXE39)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ZINC OXIDE (UNII: SOI2LOH54Z)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 37000-352-50	1 in 1 CARTON	12/16/2013	10/02/2021
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 37000-352-10	1 in 1 CARTON	12/16/2013	10/28/2021
2		100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 37000-352-15	15 mL in 1 POUCH; Type 0: Not a Combination Product	11/01/2016	07/31/2021
4	NDC: 37000-352-60	600 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/01/2016	08/01/2020
5	NDC: 37000-352-06	0.6 mL in 1 POUCH; Type 0: Not a Combination Product	07/15/2017	05/22/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part352	12/16/2013	10/28/2021

Labeler - The Procter & Gamble Manufacturing Company (004238200)