OLAY REGENERIST WHIP ACTIVE MOISTURIZER BROAD SPECTRUM SPF 25 SUNSCREEN TESTER- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream

Olay Regenerist Whip Active Moisturizer Broad Spectrum SPF 25 Sunscreen TESTER by

Drug Labeling and Warnings

Olay Regenerist Whip Active Moisturizer Broad Spectrum SPF 25 Sunscreen TESTER 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 8.0%	Sunscreen
Octisalate 4.0%	Sunscreen
Octocrylene 5.0%	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, tapioca starch, glycerin, niacinamide, dimethicone, palmitoyl pentapeptide-4, sodium hyaluronate, panthenol, sodium polyacrylate starch, stearyl alcohol, caprylyl glycol, behenyl alcohol, 1,2-hexanediol, phenoxyethanol, cetyl alcohol, dimethiconol, PEG-100 stearate, fragrance, polymethylsilsesquioxane, ceratonia siliqua (carob) fruit extract, cetearyl glucoside, cetearyl alcohol, disodium EDTA, stearic acid, palmitic acid.

Questions or comments?

Call 1-800-285-5170

SPL UNCLASSIFIED SECTION

Distr. by PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 48 g Pump

TESTER

OLAY

REGENERIST

WHIP

ACTIVE MOISTURIZER

WITH SUNSCREEN

BROAD SPECTRUM SPF 25

NET WT 48 g (1.7 oz)

INGREDIENTS AND APPEARANCE

OLAY REGENERIST WHIP ACTIVE MOISTURIZER BROAD SPECTRUM SPF 25 SUNSCREEN TESTER 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-421
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	8 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CAROB (UNII: 5MG5Z946UO)
STARCH, TAPIOCA (UNII: 24SC3U704I)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
PANTHENOL (UNII: WV9CM0O67Z)
PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
PEG-100 STEARATE (UNII: YD01N1999R)
DOCOSANOL (UNII: 9G1OE216XY)
CETYL ALCOHOL (UNII: 936JST6JCN)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-421-48	48 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/07/2020

Labeler - The Procter & Gamble Manufacturing Company (004238200)