COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20

COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20

Drug Labeling and Warnings

Drug Details

k">

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.

----------

COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20

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

COVERGIRL

OUTLAST ACTIVE

24 HR FOUNDATION +

OCTINOXATE SUNSCREEN

BROAD SPECTRUM SPF20

30 mL (1 FL OZ)

800.jpg802.jpg805.jpg810.jpg820.jpg825.jpg832.jpg840.jpg842.jpg845.jpg850.jpg855.jpg857.jpg

back

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
WATER (UNII: 059QF0KO0R)  
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)  
LAURETH-7 (UNII: Z95S6G8201)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
TALC (UNII: 7SEV7J4R1U)  
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
GLYCERIN (UNII: PDC6A3C0OX)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
TRIBEHENIN (UNII: 8OC9U7TQZ0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
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: 3/2019
 
Noxell Corporation


© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.