COVERGIRL OUTLAST EXTREME WEAR 3-IN-1 FOUNDATION 24 HR FULL COVERAGE SPF 18 OCTINOXATE SUNSCREEN LIQUID FOUNDATION- octinoxate emulsion

Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation by

Drug Labeling and Warnings

Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation by is a Otc medication manufactured, distributed, or labeled by Noxell Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Octinoxate 3.0%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures

(see Directions), decreases the risk of skin cancer and early aging caused by the sun.

Warnings

Skin Cancer/Skin Aging Alert; ;Spending time inthesunincreasesyourriskofskincancerand earlyskinaging.Thisproducthasbeenshown only to help prevent sunburn, not skin cancer or early skin aging.

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 doctor if

• rash occurs.

Keep out of reach of children.

If swollowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 15 minutes before sun exposure
• useawaterresistantsunscreenif swimming or sweating
• reapply at least every 2 hours
• children under 6 months of age: Ask a doctor
• 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 witha Broad SpectrumSPF valueof 15 or higher and other sun protection measures including:
• limit time in the sun,especially from 10 a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses.

Other information

• protect the product in this container from excessive heat and direct sun.

Inactive ingredients

CYCLOPENTASILOXANE, AQUA/WATER/EAU, TALC, BUTYLENE GLYCOL, CETYL PEG/PPG-10/1 DIMETHICONE, ACRYLATES CROSSPOLYMER, TRIMETHYLSILOXYSILICATE, CETEARYL ETHYLHEXANOATE, DIMETHICONE/ VINYL DIMETHICONE CROSSPOLYMER, MAGNESIUM SULFATE, BIS-PEG/PPG-14/ 14 DIMETHICONE, AMMONIUM

ACRYLATES COPOLYMER, TRIBEHENIN, DISTEARDIMONIUM HECTORITE, LAURETH-7, LECITHIN, TRIETHOXYCAPRYLYLSILANE, PHENOXYETHANOL, TRIHYDROXYSTEARIN, CHLORPHENESIN, PROPYLENE CARBONATE, ALCOHOL DENAT., DIMETHICONOL, XANTHAN GUM, GLYCERIN, DISODIUM EDTA, TOCOPHERYL ACETATE, DISODIUM DECETH-6 SULFOSUCCINATE, LAURETH-30, SODIUM PCA, UREA, SODIUM DEHYDROACETATE, TREHALOSE, HEXYLENE GLYCOL, POLYQUATERNIUM-51, BHT, CAPRYLYL GLYCOL, TRIACETIN, SODIUM HYALURONATE, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, [MAY CONTAIN/PEUT CONTENIR/+/-: IRON OXIDES (CI 77491, CI 77492, CI 77499), TITANIUM DIOXIDE (CI 77891)].

Questions or comments?

Call 1-800-426-8374

Package Label

INGREDIENTS AND APPEARANCE

COVERGIRL OUTLAST EXTREME WEAR 3-IN-1 FOUNDATION 24 HR FULL COVERAGE SPF 18 OCTINOXATE SUNSCREEN LIQUID FOUNDATION 
octinoxate emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22700-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
GLYCERIN (UNII: PDC6A3C0OX)
(4-NITROPHENYL)UREA (UNII: DY0F0348GL)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
LAURETH-30 (UNII: W9D845551A)
TREHALOSE (UNII: B8WCK70T7I)
BHT (UNII: 1P9D0Z171K)
CHLORPHENESIN (UNII: I670DAL4SZ)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
SODIUM PCA (UNII: 469OTG57A2)
LAURETH-7 (UNII: Z95S6G8201)
TALC (UNII: 7SEV7J4R1U)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
IRON OXIDES (UNII: 1K09F3G675)
TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
MAGNESIUM SULFATE (UNII: DE08037SAB)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
TRIACETIN (UNII: XHX3C3X673)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
XANTHAN GUM (UNII: TTV12P4NEE)
DISODIUM DECETH-6 SULFOSUCCINATE (UNII: SX9Q9F5YWB)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22700-030-01	1 in 1 CARTON	12/01/2021
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/01/2021

Labeler - Noxell Corporation (003082997)

Establishment
Name	Address	ID/FEI	Business Operations
Noxell Corporation		003082997	manufacture(22700-030)