COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20- octinoxate liquid 
Noxell Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20

Active ingredent

Octinoxate 3%

Purpose

Sunscreen

Uses

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

Other information

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

COVERGIRL

OUTLAST ACTIVE

24 HR FOUNDATION +

OCTINOXATE SUNSCREEN

BROAD SPECTRUM SPF20

30 mL (1 FL OZ)

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6062657075

COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20 
octinoxate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22700-156
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
LAURETH-7 (UNII: Z95S6G8201)  
BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
TRIACETIN (UNII: XHX3C3X673)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22700-156-8030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
2NDC:22700-156-0230 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
3NDC:22700-156-0530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
4NDC:22700-156-1030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
5NDC:22700-156-2030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
6NDC:22700-156-2530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
7NDC:22700-156-3230 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
8NDC:22700-156-4030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
9NDC:22700-156-4230 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
10NDC:22700-156-4530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
11NDC:22700-156-5030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
12NDC:22700-156-5530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
13NDC:22700-156-5730 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
14NDC:22700-156-6030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
15NDC:22700-156-6230 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
16NDC:22700-156-6530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
17NDC:22700-156-7030 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
18NDC:22700-156-7530 mL in 1 TUBE; Type 0: Not a Combination Product03/11/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/11/2019
Labeler - Noxell Corporation (003082997)
Establishment
NameAddressID/FEIBusiness Operations
Noxell Corporation003082997manufacture(22700-156)

Revised: 1/2023
Document Id: f3063fc6-c025-376b-e053-2a95a90af3c9
Set id: 83d3c09f-d91a-4025-e053-2991aa0a7ff0
Version: 4
Effective Time: 20230124
 
Noxell Corporation