COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20- octinoxate liquid

Covergirl Outlast Active Foundation SPF 20 by

Drug Labeling and Warnings

Covergirl Outlast Active Foundation SPF 20 by is a Otc medication manufactured, distributed, or labeled by Noxell Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredent

Octinoxate 3%

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 skin 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 a 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 the 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

Cyclopentasiloxane, Aqua/Water/Eau, Butylene Glycol, Talc, Cetyl PEG/PPG-10/1 Dimethicone,

Trimethylsiloxysilicate, Acrylates Crosspolymer, Cetearyl Ethylhexanoate, Ammonium Acrylates Copolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Magnesium Sulfate, Bis-PEG/PPG-14/14 Dimethicone, Polymethyl Methacrylate, Tribehenin, Disteardimonium Hectorite, Laureth-7, Lecithin, Phenoxyethanol, Trihydroxystearin, Chlorphenesin, Triethoxycaprylylsilane, Parfum/Fragrance, Alcohol Denat., Propylene Carbonate, Dimethiconol, Xanthan Gum, Glycerin, Disodium Deceth-6 Sulfosuccinate, Disodium EDTA, Tocopheryl Acetate, Laureth-30, Sodium PCA , Urea, Hexyl Cinnamal, Sodium Dehydroacetate, Limonene, Trehalose, Butylphenyl Methylpropional, Benzyl Salicylate, Hexylene Glycol, Linalool, Geraniol, Polyquaternium-51, BHT, Citronellol, Alpha-Isomethyl Ionone, 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?

1-800-426-8374

PRINCIPAL DISPLAY PANEL

COVERGIRL

OUTLAST ACTIVE

24 HR FOUNDATION +

OCTINOXATE SUNSCREEN

BROAD SPECTRUM SPF20

30 mL (1 FL OZ)

INGREDIENTS AND APPEARANCE

COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20 
octinoxate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22700-156
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURETH-7 (UNII: Z95S6G8201)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
TRIACETIN (UNII: XHX3C3X673)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TALC (UNII: 7SEV7J4R1U)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
CHLORPHENESIN (UNII: I670DAL4SZ)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
GLYCERIN (UNII: PDC6A3C0OX)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22700-156-80	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
2	NDC: 22700-156-02	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
3	NDC: 22700-156-05	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
4	NDC: 22700-156-10	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
5	NDC: 22700-156-20	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
6	NDC: 22700-156-25	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
7	NDC: 22700-156-32	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
8	NDC: 22700-156-40	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
9	NDC: 22700-156-42	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
10	NDC: 22700-156-45	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
11	NDC: 22700-156-50	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
12	NDC: 22700-156-55	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
13	NDC: 22700-156-57	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
14	NDC: 22700-156-60	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
15	NDC: 22700-156-62	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
16	NDC: 22700-156-65	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
17	NDC: 22700-156-70	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019
18	NDC: 22700-156-75	30 mL in 1 TUBE; Type 0: Not a Combination Product	03/11/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/11/2019

Labeler - Noxell Corporation (003082997)

Establishment
Name	Address	ID/FEI	Business Operations
Noxell Corporation		003082997	manufacture(22700-156)