Label: COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20- octinoxate liquid
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NDC Code(s):
22700-156-02,
22700-156-05,
22700-156-10,
22700-156-20, view more22700-156-25, 22700-156-32, 22700-156-40, 22700-156-42, 22700-156-45, 22700-156-50, 22700-156-55, 22700-156-57, 22700-156-60, 22700-156-62, 22700-156-65, 22700-156-70, 22700-156-75, 22700-156-80
- Packager: Noxell Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated January 24, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredent
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
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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
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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?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COVERGIRL OUTLAST ACTIVE FOUNDATION SPF 20
octinoxate liquidProduct 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 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 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)
