Home › NDC Lookup › Ingredients › Octisalate, Titanium Dioxide › 61957-3441-00
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7W Warm OCTISALATE, TITANIUM DIOXIDE 35 mg/mL; 9.4 mg/mL Emulsion — NDC 61957-3441-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7W Warm OCTISALATE, TITANIUM DIOXIDE 35 mg/mL; 9.4 mg/mL Emulsion — NDC 61957-3441-0 (Billing 61957-3441-00)

by Parfums Christian Dior · 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE

This is a package of Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7W Warm OCTISALATE, TITANIUM DIOXIDE 35 mg/mL; 9.4 mg/mL Emulsion from Parfums Christian Dior, marketed since Mar 2026 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 61957-3441-00
🏷️ FDA NDC (as labeled) 61957-3441-0 billing pads the package segment with a zero
This package
Contains30 mL in 1 bottle Pack sizes2 compare ↓
Main listing for product 61957-3441 · Also comes in: 20 mL 61957-3441-1
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 61957-3441-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
61957 labeler · 3441 product · 0 package
Package marketed since
Mar 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
3348901797511, 3348901799331
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61957-3441-0
Product NDC 61957-3441
11-digit billing NDC 61957344100
UNII 4X49Y0596W, 15FIX9V2JP
UPC 3348901797511, 3348901799331
Application # M020
SPL Set ID 262b4cfc-71c3-485e-906f-a88fe33035a8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-01
Route TOPICAL
Dosage form EMULSION
Substance OCTISALATE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 61957-3441-0 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 61957-3441-00. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is a topical foundation emulsion marketed as an OTC monograph sunscreen product. It contains octisalate and titanium dioxide, which are active ingredients typically used as ultraviolet (UV) filters in sunscreen formulations. Octisalate is a chemical UV absorber, while titanium dioxide is a mineral UV reflectant. Together, these ingredients function to help protect skin from sun exposure when applied to the face as directed.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 20 mL
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
61957-3441-00 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE 2026-03-01 — Active
61957-3441-01 61957-3441-1 1 BOTTLE in 1 CARTON / 20 mL in 1 BOTTLE 2026-03-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle in 1 carton / 30 ml in 1 bottle.
What NDC number is used to bill for this package of Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7W Warm OCTISALATE, TITANIUM DIOXIDE 35 mg/mL; 9.4 mg/mL Emulsion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 0.5C 35 mg/mL; 9.4 mg/mL 49817-2063-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 0.5N 35 mg/mL; 9.4 mg/mL 49817-2064-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 0N 35 mg/mL; 9.4 mg/mL 49817-2065-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 1.5N 35 mg/mL; 9.4 mg/mL 49817-2066-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 1C 35 mg/mL; 9.4 mg/mL 49817-2067-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 1N 35 mg/mL; 9.4 mg/mL 49817-2068-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 2N 35 mg/mL; 9.4 mg/mL 49817-2069-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 2W 35 mg/mL; 9.4 mg/mL 49817-2070-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 3.5N 35 mg/mL; 9.4 mg/mL 49817-2071-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 3N 35 mg/mL; 9.4 mg/mL 49817-2072-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 3W 35 mg/mL; 9.4 mg/mL 49817-2073-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 4N 35 mg/mL; 9.4 mg/mL 49817-2074-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 4W 35 mg/mL; 9.4 mg/mL 49817-2075-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 5N 35 mg/mL; 9.4 mg/mL 49817-2076-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 6N 35 mg/mL; 9.4 mg/mL 49817-2077-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 7N 35 mg/mL; 9.4 mg/mL 49817-2078-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 8N 35 mg/mL; 9.4 mg/mL 49817-2079-01 Guerlain 35 ml — — FDA listed —
Parure Gold Skin Matte Foundation No-Transfer High Perfection 24H Care And Wear Infused With 24K Gold And White Peony With Sunscreen Broadspectrum Spf 15 0C 35 mg/mL; 9.4 mg/mL 49817-2080-01 Guerlain 35 ml — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 5N Neutral 35 mg/mL; 9.4 mg/mL 61957-3433-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 6N Neutral 35 mg/mL; 9.4 mg/mL 61957-3437-00 Parfums 1 bottle — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 7.5N 35 mg/mL; 9.4 mg/mL 61957-3005-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 7W 35 mg/mL; 9.4 mg/mL 61957-3003-00 Parfums 30 ml — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7,5N Neutral 35 mg/mL; 9.4 mg/mL 61957-3439-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7N Neutral 35 mg/mL; 9.4 mg/mL 61957-3440-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 9N Neutral 35 mg/mL; 9.4 mg/mL 61957-3443-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 6,5W Warm 35 mg/mL; 9.4 mg/mL 61957-3436-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 6W Warm 35 mg/mL; 9.4 mg/mL 61957-3438-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 7W Warm 35 mg/mL; 9.4 mg/mLthis 61957-3441-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 10N Neutral 35 mg/mL; 9.4 mg/mL 61957-3444-00 Parfums 1 bottle — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 6N 35 mg/mL; 9.4 mg/mL 61957-3007-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 9N 35 mg/mL; 9.4 mg/mL 61957-3001-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 6W 35 mg/mL; 9.4 mg/mL 61957-3006-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 6.5W 35 mg/mL; 9.4 mg/mL 61957-3008-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 6.5N 35 mg/mL; 9.4 mg/mL 61957-3009-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 5W 35 mg/mL; 9.4 mg/mL 61957-3010-00 Parfums 30 ml — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 wless Skin True Foundation SPF 20 8N Neutral 35 mg/mL; 9.4 mg/mL 61957-3442-00 Parfums 1 bottle — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 8N 35 mg/mL; 9.4 mg/mL 61957-3002-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 7N 35 mg/mL; 9.4 mg/mL 61957-3004-00 Parfums 30 ml — — FDA listed —
FOREVER Transfer-proof - 24h foundation High perfection Concentrated floral skincare with sunscreen Broad spectrum SPF 15 5N 35 mg/mL; 9.4 mg/mL 61957-3011-00 Parfums 30 ml — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 6,5N Neutral 35 mg/mL; 9.4 mg/mL 61957-3435-00 Parfums 1 bottle — — FDA listed —
Dior Forever Skin Wear Flawless Skin True Foundation SPF 20 5W Warm 35 mg/mL; 9.4 mg/mL 61957-3434-00 Parfums 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2026
On the market since
Mar 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII L4EL31FWIL
    A synthetic peptide (short chain of amino acids) used as a conditioning or texture-enhancing agent in topical formulations. It helps improve product feel and skin compatibility in creams and lotions.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII M30XO5X4XD
    A dried plant root extract from Florentine iris used as a natural fragrance, flavoring, and binding agent in medications. It helps hold tablet ingredients together and adds mild pleasant taste or aroma.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII X33R8U0062
    Isostearic acid is a fatty acid derived from vegetable oils. It acts as an emulsifier and lubricant in medicines, helping blend ingredients together and reducing friction during tablet or capsule manufacturing.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII S73ZQI0GXM
    Methyl trimethicone is a silicone-based lubricant and glidant used in tablets and capsules. It reduces friction between particles and equipment during manufacturing, helping the medicine flow smoothly and compress evenly.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII Z52UR6Z5AB
    A synthetic compound made from glycerin and stearic acid derivatives, used as an emulsifier and thickener in topical formulations to help blend oil and water ingredients together and improve texture.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII AYU7QD893W
    A naturally-derived amino acid compound used as an emulsifier and surfactant. It helps blend oil and water-based ingredients together and improves the product's texture and stability.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII 023C2WHX2V
    Tromethamine is a chemical buffer that helps maintain the proper acidity level in liquid medicines. It neutralizes acids and stabilizes the solution so the medication remains effective and safe throughout its shelf life.
  • UNII RGT30824HY
    A plant extract from the nasturtium flower used as a natural coloring agent and flavoring ingredient in medicines and supplements.
  • UNII 9NH1UDD2RR
    A synthetic silicone polymer that forms a smooth, water-resistant film. Used in topical formulations as a skin protectant coating and to improve product texture and spreadability on the skin.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

27 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAQUA (WATER) • METHYL TRIMETHICONE • ALCOHOL • ISODODECANE • PEG-10 DIMETHICONE • TRIMETHYLSILOXYSILICATE • BUTYLENE GLYCOL • METHYL METHACRYLATE CROSSPOLYMER • DIMETHICONE • DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER • VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER • CETYL DIMETHICONE • DISTEARDIMONIUM HECTORITE • NIACINAMIDE • POLYGLYCERYL-10 DECAISOSTEARATE • SODIUM MYRISTOYL GLUTAMATE • PARFUM (FRAGRANCE) • PROPYLENE CARBONATE • CHLORPHENESIN • POLYHYDROXYSTEARIC ACID • CAPRYLICA/CAPRIC TRIGLYCERIDE • ALUMINUM HYDROXIDE • HYALURONIC ACID • TROMETHAMINE • ISOSTEARIC ACID • ALUMINA • STEARIC ACID • TOCOPHEROL • POLYGLYCERYL-3 POLYRICINOLEATE • LECITHIN • PENTYLENE GLYCOL • IRIS FLORENTINA ROOT EXTRACT • TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT • SODIUM BENZOATE • POTASSIUM SORBATE • ACETYL HEXAPEPTIDE-8 [MAY CONTAIN: CI 77491 (IRON OXIDES), CI 77492 (IRON OXIDES), CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)]. N° 22157/Z

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerParfums Christian Dior
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code61957
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio224 products on file

More NDCs from Parfums Christian Dior labeler code 61957

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 31 words ▾

Uses Helps prevent sunburn. If used as directed with other sun protection measures ( see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 91 words ▾

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 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-sleeve shirts, pants, hats, and sunglasses.

Children under 6 months of age: ask a doctor.

⚠️ Warnings 54 words ▾

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

🧪 Active Ingredient 9 words ▾

Active ingredients Octisalate 3.50% Titanium Dioxide 0.94% Purpose Sunscreen

🧪 Inactive Ingredients 132 words ▾

Inactive ingredients AQUA (WATER) • METHYL TRIMETHICONE • ALCOHOL • ISODODECANE • PEG-10 DIMETHICONE • TRIMETHYLSILOXYSILICATE • BUTYLENE GLYCOL • METHYL METHACRYLATE CROSSPOLYMER • DIMETHICONE • DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER • VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER • CETYL DIMETHICONE • DISTEARDIMONIUM HECTORITE • NIACINAMIDE • POLYGLYCERYL-10 DECAISOSTEARATE • SODIUM MYRISTOYL GLUTAMATE • PARFUM (FRAGRANCE) • PROPYLENE CARBONATE • CHLORPHENESIN • POLYHYDROXYSTEARIC ACID • CAPRYLICA/CAPRIC TRIGLYCERIDE • ALUMINUM HYDROXIDE • HYALURONIC ACID • TROMETHAMINE • ISOSTEARIC ACID • ALUMINA • STEARIC ACID • TOCOPHEROL • POLYGLYCERYL-3 POLYRICINOLEATE • LECITHIN • PENTYLENE GLYCOL • IRIS FLORENTINA ROOT EXTRACT • TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT • SODIUM BENZOATE • POTASSIUM SORBATE • ACETYL HEXAPEPTIDE-8 [MAY CONTAIN : CI 77491 (IRON OXIDES), CI 77492 (IRON OXIDES) , CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)].

N° 22157/Z

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin.

📄 When Using This Product 13 words ▾

When using this product, keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if rash occurs.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 10 words ▾

Package Labeling: 1047

Package Labeling: Outer Package08 Inner Package08 Box08

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for OCTISALATE, TITANIUM DIOXIDE — the ingredient across all brands.

Top reported reactions

Dysphagia1
Dyspnoea1
Erythema1
Pain1
Pruritus1
Swelling1
Urticaria1

Reporter sex

2 reports
Female · 100%

Serious outcomes

Life-threatening1
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Parfums Christian Dior. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 bottle (61957-3441-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Parfums Christian Dior is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 61957-3440-00 · Parfums 61957-3442-00 · Parfums →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.