Medicine guide

Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 Hr Full Coverage Spf 18 Octinoxate Sunscreen Liquid Foundation

30 mg/mL · Emulsion

  • Available without prescription
Active substance
Octinoxate
Made by
Noxell Corporation

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2024-11-21

What it is

Sunscreen

Used for
  • 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.
Do not take it if

On damaged or broken skin.

All warnings ↓
Good to know
  • Sold without a prescription
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
88other products contain Octinoxate — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

  • 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.

From the official label · 2024-11-21 · DailyMed

Do not take it if

on damaged or broken skin.

Quoted from the official label, section “OTC — Do Not Use”.

How to take it

These directions are for this exact strength and form. Another one is different.

  • 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.

Quoted from the official label, section “Dosage & Administration”.

Stop and get help if

and ask doctor if rash occurs.

Quoted from the official label, section “OTC — Stop Use”.

Other 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.
  • keep out of eyes. Rinse with water to remove.

Quoted from the official label, section “Warnings”.

Keep away from children

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

Quoted from the official label, section “OTC — Keep Out of Reach of Children”.

How to store it

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

Quoted from the official label, section “Storage and Handling”.

What kind of medicine it is

Sunscreen

Quoted from the official label, section “OTC — Purpose”.

Other ingredients

Relevant if you react to a dye, a preservative, lactose or gluten.

  • 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)].

Quoted from the official label, section “Inactive Ingredients”.

Questions about this product

Call 1-800-426-8374

Quoted from the official label, section “OTC — Questions”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

  • Alcohol (ethanol)ALCOHOL DENATMatters for children, in pregnancy, in recovery and with some medicines.
  • SoyLECITHINMatters with a soy allergy.
  • Titanium dioxideTITANIUM DIOXIDE (CI 77891)]A whitening agent no longer allowed in food in the EU (E171).

Quoted from the FDA label. A label that does not name an ingredient is not a guarantee that the product is free of it, and formulations change. With an allergy, check the pack and ask a pharmacist.

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

CanadaNo exact match for this strength and form

Details

Made byNoxell Corporation
Active substanceOctinoxate
Strength30 mg/mL
FormEmulsion
RouteTopical
Packs1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
NDC22700-030

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.