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CAPTURE TOTALE C.E.L.L. ENERGY SUPER POTENT SERUM FOUNDATION BROAD SPECTRUM SPF 20 0N ENSULIZOLE, OCTISALATE 27 mg/mL; 45 mg/mL Emulsion, 30 mL — NDC 61957-2400-00 package photo

CAPTURE TOTALE C.E.L.L. ENERGY SUPER POTENT SERUM FOUNDATION BROAD SPECTRUM SPF 20 0N ENSULIZOLE, OCTISALATE 27 mg/mL; 45 mg/mL Emulsion, 30 mL

by Parfums Christian Dior · 30 mL in 1 BOTTLE (61957-2400-0)
NDC 61957-2400-00
🏷️ FDA NDC (as labeled) 61957-2400-0 billing pads the package segment with a zero
This package
Contains30 mL Pack sizes2 compare ↓
Also comes in: 20 ml 61957-2400-01
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 61957-2400-0
Product NDC 61957-2400
11-digit billing NDC 61957240000
UNII 9YQ9DI1W42, 4X49Y0596W
UPC 3348901549202
Application # M020
SPL Set ID 31141a45-54e2-4463-ab42-4df56d911650
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-09-01
Route TOPICAL
Dosage form EMULSION
Substance ENSULIZOLE; OCTISALATE
Why two NDCs? The FDA registers this code as 61957-2400-0 — 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 → 61957-2400-00. 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.

🏭 Manufacturer & labeler

LabelerParfums Christian Dior
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code61957
First marketedSep 2021
Product typeHuman Otc Drug
Portfolio224 products on file
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.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter monograph cosmetic emulsion applied to skin that combines a foundation with sun protection. Ensulizole and octisalate are ultraviolet (UV) filters that are typically used in sunscreen products to help protect skin from UVA and UVB radiation. The product is formulated as a liquid-to-powder emulsion intended for facial use and carries a broad spectrum SPF 20 rating.

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.

🧪 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 K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII OSF83Q896J
    A plant-derived ingredient from the seeds of Aframomum angustifolium, a West African spice plant. It's used in medicines as a flavoring agent to improve taste and sometimes as a natural preservative.
  • 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 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • 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 H895X08VNQ
    A silicone-based polymer that forms small, hard particles. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII OSA9UP217S
    Dimethiconol is a silicone-based lubricant and anti-foaming agent. It reduces friction between tablet components and prevents foam formation during manufacturing and storage.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 4QGR4P2YOI
    A silicone-based lubricant that reduces friction between tablet particles and manufacturing equipment. It helps tablets flow smoothly during production and prevents them from sticking together or to machinery.
  • UNII 1394NXB9L6
    A plant-derived protein from soybeans that has been broken down into smaller pieces using enzymes. It acts as a binder and texture agent, helping hold ingredients together and improve the product's consistency and mouthfeel.
  • UNII 0Q8K841432
    A plant extract from jasmine flowers used as a fragrance and flavoring agent in medicines. It adds pleasant scent and taste to make the medication more appealing to take.
  • UNII 25G622K2RA
    A silicone-based surfactant that helps blend oil and water in cosmetic or topical formulations. It reduces surface tension to improve product spreadability and texture.
  • UNII YK3DC63Y5M
    A mineral compound derived from natural or synthetic sources that acts as an anti-caking agent and flow aid. It helps prevent clumping and improves the powder's ability to flow smoothly during manufacturing and tablet formation.
  • 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 V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII 3Z3866YW6P
    A plant extract from peony root used in traditional herbal formulations. It may function as a flavoring agent, natural colorant, or botanical ingredient to support the product's herbal composition.
  • UNII 7832HOY4ZQ
    A red seaweed extract used as a thickener and stabilizer in liquid medicines and suspensions. It helps maintain consistent texture and keeps ingredients evenly mixed throughout the product.
  • 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 DR0K5NOJ4R
    Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII WN66R7GL93
    A modified form of hyaluronic acid, a naturally occurring substance that holds water. Used as a thickener, lubricant, and moisture-retaining agent in formulations, especially in topical or injectable products.
  • 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • 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 0W8RRI5W5A
    A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
  • 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 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.
  • UNII VCQ006KQ1E
    Xylitol is a naturally occurring sugar alcohol derived from plants. It's used in medicines as a sweetener, bulking agent, and to improve taste, especially in liquid formulations and chewable tablets.

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

The official label also states• AQUA (WATER) • DIMETHICONE • METHYL TRIMETHICONE • LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • PHENYL TRIMETHICONE • SYNTHETIC FLUOROPHLOGOPITE • GLYCERIN • PENTYLENE GLYCOL • SILICA • BUTYLENE GLYCOL• SORBITAN SESQUIOLEATE • TROMETHAMINE • ACRYLATES/DIMETHICONE COPOLYMER • MICA • DIMETHICONOL • PARFUM (FRAGRANCE) • SODIUM MYRISTOYL GLUTAMAT • GLYCERYL UNDECYL DIMETHICONE • CHLORPHENESIN • CAPRYLYL GLYCOL• SODIUM CHLORIDE • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • POLYSORBATE 80 • HYDROGEN DIMETHICONE • ALUMINUM HYDROXIDE • ADENOSINE• SODIUM ACETYLATED HYALURONATE • XYLITOL • TOCOPHEROL • SODIUM SURFACTIN • AFRAMOMUM ANGUSTIFOLIUM SEED EXTRACT • PALMARIA PALMATA EXTRACT • SODIUM BENZOATE • HYDROLYZED SOY PROTEIN • PAEONIA LACTIFLORA ROOT EXTRACT • JASMINUM OFFICINALE (JASMINE) FLOWER EXTRACT. [MAY CONTAIN:CI 77491,CI 77492,CI 77499 (IRON OXIDES) • CI 77891 (TITANIUM DIOXIDE) • CI 77947 (ZINC OXIDE)]. N°15310/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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 1N 27 mg/mL; 45 mg/mL 61957-2401-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 1,5N 27 mg/mL; 45 mg/mL 61957-2402-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 2N 27 mg/mL; 45 mg/mL 61957-2403-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 2Cr 27 mg/mL; 45 mg/mL 61957-2404-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 2W 27 mg/mL; 45 mg/mL 61957-2405-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 3N 27 mg/mL; 45 mg/mL 61957-2406-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 4N 27 mg/mL; 45 mg/mL 61957-2407-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 5N 27 mg/mL; 45 mg/mL 61957-2408-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 6N 27 mg/mL; 45 mg/mL 61957-2409-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 7N 27 mg/mL; 45 mg/mL 61957-2410-00 Parfums 30 ml — — FDA listed —
Capture Totale C.e.l.l. Energy Super Potent Serum Foundation Broad Spectrum Spf 20 0N 27 mg/mL; 45 mg/mLthis 61957-2400-00 Parfums 30 ml — — 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

🏛️
2021
On the market since
Sep 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
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.

🔬 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 ENSULIZOLE, OCTISALATE — the ingredient across all brands.

Top reported reactions

Application Site Pain3
Application Site Erythema1
Application Site Irritation1
Application Site Rash1
Drug Ineffective For Unapproved Indication1

Reporter sex

4 reports
Male · 25%
Female · 75%

Serious outcomes

Disabling1
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 2 0
Most recent year is provisional (FAERS lags ~3 months).
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
61957-2400-00 You're viewing this 30 mL in 1 BOTTLE (61957-2400-0) 2021-09-01 Active
61957-2400-01 20 mL in 1 TUBE (61957-2400-1) 2021-09-01 Discontinued by firm

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 61957-2400-00?
NDC 61957-2400-00 contains 30 mL — 30 ml in 1 bottle.
What is the difference between NDC 61957-2400-00 and NDC 61957-2400-01?
Both are CAPTURE TOTALE C.E.L.L. ENERGY SUPER POTENT SERUM FOUNDATION BROAD SPECTRUM SPF 20 0N ENSULIZOLE, OCTISALATE 27 mg/mL; 45 mg/mL Emulsion — the drug itself is identical. NDC 61957-2400-00 is the 30 mL package, while NDC 61957-2400-01 is the 20 ml package.
What NDC number is used to bill for this package of CAPTURE TOTALE C.E.L.L. ENERGY SUPER POTENT SERUM FOUNDATION BROAD SPECTRUM SPF 20 0N ENSULIZOLE, OCTISALATE 27 mg/mL; 45 mg/mL Emulsion?
Bill NDC 61957-2400-00 — the 11-digit billing format is 61957240000. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 61957-2400-0, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 61957-2400-00, written without dashes as 61957240000. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 61957-2400-00, the first segment (61957) is the labeler code FDA assigned to Parfums Christian Dior; the middle segment (2400) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) identifies this exact package size and type. Together they name one specific package of one specific product.
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 20 ml (61957-2400-01). 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.

📄 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
🎯 Indications and Usage 31 words ▾

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

⏱️ 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.

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: Sun Protection Measures. 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 10 words ▾

Active ingredients Ensulizole 2.70 % Octisalate 4.50 % Purpose Sunscreen

🧪 Inactive Ingredients 130 words ▾

Inactive ingredients • AQUA (WATER) • DIMETHICONE • METHYL TRIMETHICONE • LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • PHENYL TRIMETHICONE • SYNTHETIC FLUOROPHLOGOPITE • GLYCERIN • PENTYLENE GLYCOL • SILICA • BUTYLENE GLYCOL• SORBITAN SESQUIOLEATE • TROMETHAMINE • ACRYLATES/DIMETHICONE COPOLYMER • MICA • DIMETHICONOL • PARFUM (FRAGRANCE) • SODIUM MYRISTOYL GLUTAMAT • GLYCERYL UNDECYL DIMETHICONE • CHLORPHENESIN • CAPRYLYL GLYCOL• SODIUM CHLORIDE • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • POLYSORBATE 80 • HYDROGEN DIMETHICONE • ALUMINUM HYDROXIDE • ADENOSINE• SODIUM ACETYLATED HYALURONATE • XYLITOL • TOCOPHEROL • SODIUM SURFACTIN • AFRAMOMUM ANGUSTIFOLIUM SEED EXTRACT • PALMARIA PALMATA EXTRACT • SODIUM BENZOATE • HYDROLYZED SOY PROTEIN • PAEONIA LACTIFLORA ROOT EXTRACT • JASMINUM OFFICINALE (JASMINE) FLOWER EXTRACT. [MAY CONTAIN:CI 77491,CI 77492,CI 77499 (IRON OXIDES) • CI 77891 (TITANIUM DIOXIDE) • CI 77947 (ZINC OXIDE)].

N°15310/Z

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61957-2303-00 · Parfums 61957-2401-00 · 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.