FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20

OCTINOXATE AND TITANIUM DIOXIDE TOPICAL HUMAN OTC DRUG

FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 is an FDA drug label for the active ingredient OCTINOXATE AND TITANIUM DIOXIDE manufactured by ESTEE LAUDER INC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260609.

Generic name
OCTINOXATE AND TITANIUM DIOXIDE
Manufacturer
ESTEE LAUDER INC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
11559-066
Application
M020
Label effective
20260609

About this product

FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 is an FDA-registered drug product whose active ingredient is OCTINOXATE AND TITANIUM DIOXIDE. It is labelled by ESTEE LAUDER INC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 11559-066, application M020, label effective 20260609. It is one of 11 FDA drug label records sharing the active ingredient OCTINOXATE AND TITANIUM DIOXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing OCTINOXATE AND TITANIUM DIOXIDE are most often described in connection with: helps prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients Octinoxate 4% Titanium dioxide 1.5%

Indications & Usage

Use Helps prevent sunburn

Dosage & Administration

Direction Adults, 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 of age: ask a doctor

Warnings

Warnings For external use only Do not use on on damaged or broken skin When using this product avoid contact with eyes. If contact occurs, rinse throughly with water. Stop use and ask a doctor if rash occurs Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

More products with the same ingredient

OCTINOXATE AND TITANIUM DIOXIDE

LOreal Paris Infallible Up to 24 H Fresh Wear Foundation Broad Spectrum SPF 25 Sunscreen

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Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Broad Spectrum SPF 25 Sunscreen

SICOS ET CIE View label

Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Broad Spectrum SPF 25 Sunscreen

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How products containing OCTINOXATE AND TITANIUM DIOXIDE compare

FDA lists 11 drug label records with OCTINOXATE AND TITANIUM DIOXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — L'Oreal USA Products Inc 5
— — SICOS ET CIE 3
— — ESTEE LAUDER INC 2
— — MAX HUBER RESEARCH LAB INC 1
— — — —

Recall and safety notices

3 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-1132-2019 Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022 Estee Lauder Inc Class III Terminated 20190424
D-1452-2014 DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France Estee Lauder Inc Class III Terminated 20140730
D-151-2013 ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets, ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01 Estee Lauder Inc Class III Terminated 20130213

Frequently asked questions

What is FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 used for?
Use Helps prevent sunburn

Who makes FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20?
ESTEE LAUDER INC is the labeler of record for FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20. 11 FDA label records share the active ingredient OCTINOXATE AND TITANIUM DIOXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing OCTINOXATE AND TITANIUM DIOXIDE?
Yes. 11 FDA drug label records list OCTINOXATE AND TITANIUM DIOXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has FUTURIST HYDRATING COLLAGEN-PEPTIDE MAKEUP BROAD SPECTRUM SPF 20 been recalled?
3 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.