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Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 6C1 Cacao avobenzone, homosalate, octisalate, and octocrylene 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL Cream — NDC 82761-0014-60 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 6C1 Cacao avobenzone, homosalate, octisalate, and octocrylene 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL Cream — NDC 82761-014-60 (Billing 82761-0014-60)

by Laura Mercier US Buyer LLC · 1 TUBE in 1 CARTON / 50 mL in 1 TUBE

This is a package of Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 6C1 Cacao avobenzone, homosalate, octisalate, and octocrylene 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL Cream from Laura Mercier US Buyer LLC, marketed since Aug 2022 and currently FDA-listed. It is this product's only package size.

NDC 82761-0014-60
🏷️ FDA NDC (as labeled) 82761-014-60 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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 82761-014-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82761 labeler · 014 product · 60 package
Package marketed since
Aug 31, 2022
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8276101460 2
FDA record last changed
Oct 1, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82761-014-60
Product NDC 82761-014
11-digit billing NDC 82761001460
UNII G63QQF2NOX, 4X49Y0596W, 5A68WGF6WM, V06SV4M95S
Application # M020
SPL Set ID e78e17bf-5606-1031-e053-2a95a90adb35
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-08-31
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 82761-014-60 — a 5-3-2 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 product segment → 82761-0014-60. 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 tinted cream moisturizer applied to the skin that contains four sunscreen active ingredients: avobenzone, homosalate, octisalate, and octocrylene. These ingredients function as ultraviolet (UV) filters and are commonly used together in sunscreen products to help protect skin from both UVA and UVB rays. The product is marketed as an over-the-counter monograph drug with a sun protection factor (SPF) of 25. It is formulated to provide moisture and a light tint while functioning as a topical sunscreen.

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 gPer 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.
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
82761-0014-60 You're viewing this Main listing 1 TUBE in 1 CARTON / 50 mL in 1 TUBE 2022-08-31 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 0N1 Petal 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0001-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 0W1 Pearl 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0002-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 1C0 Cameo 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0003-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 1W1 Porcelain 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0004-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 2N1 Nude 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0005-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 2W1 Natural 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0006-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 3N1 Sand 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0007-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 3W1 Bisque 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0008-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 4C1 Almond 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0009-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 4W1 Tawny 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0010-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 5N1 Walnut 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0011-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 5W1 Tan 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0012-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 6N1 Mocha 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mL 82761-0013-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Light Revealer Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 6C1 Cacao 1.53 g/50mL; 2.55 g/50mL; 2.55 g/50mL; 1.53 g/50mLthis 82761-0014-60 Laura 1 tube — — 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

🏛️
2022
On the market since
Aug 2022
📍
2026
Currently FDA-listed
4 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.

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 WR1WPI7EW8
    A synthetic form of vitamin E used as an antioxidant. It prevents oils and fats in the medicine from breaking down and becoming rancid, helping keep the product stable during storage.
  • UNII 168S4EO8YJ
    A seaweed extract from brown algae, used as a natural binder and thickening agent to help hold tablet ingredients together and improve product texture.
  • UNII 39YR661C4U
    A synthetic chemical compound used as a preservative in medicines to prevent bacterial and fungal growth, helping keep the product safe and effective during storage.
  • UNII X2I70H0QJE
    A silicone-based polymer made from polyethylene glycol and polypropylene glycol chains. It works as an emulsifier and surfactant, helping mix water and oil ingredients together and improving the texture and spreadability of creams, lotions, and other topical products.
  • 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 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII ICS790225B
    A plant-derived cleaning agent made from coconut oil and glucose. It works as a surfactant and emulsifier to help mix oil and water-based ingredients together in the formulation.
  • 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 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • 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 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • 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 X8725R883T
    A synthetic oily liquid derived from branched carboxylic acids, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII YD01N1999R
    A waxy substance made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and serves as an emulsifier and solubilizer in liquid and semi-solid medicines.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • 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 W8K377W98I
    A mixture of sugars made by rearranging glucose molecules. It acts as a sweetener and filler to improve taste and add bulk to the medicine while helping it hold together.
  • 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 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII KM7N50LOS6
    Tin oxide is an inorganic mineral compound used in medicines as a colorant and opacifying agent. It provides white or off-white color to tablets, capsules, and coatings while helping make formulations less transparent.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 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 TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWater, Butyloctyl Salicylate, Butylene Glycol, Octyldodecyl Neopentanoate, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Ascophyllum Nodosum Extract, Silica, Ethylhexylglycerin, Cetearyl Alcohol, Coco-Glucoside, Citric Acid, Batyl Alcohol, BIS-PEG/PPG-14/14 Dimethicone, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Potassium Hydroxide, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Xanthan Gum, Saccharide Isomerate, Sodium Citrate, Tin Oxide, Phenoxyethanol, Potassium Sorbate. May Contain: Iron Oxides, Mica, Titanium Dioxide.

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

LabelerLaura Mercier US Buyer LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code82761
First marketedAug 2022
Product typeHuman Otc Drug
Portfolio36 products on file

More NDCs from Laura Mercier US Buyer LLC labeler code 82761

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 📦 Storage and Handling 🧪 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 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 94 words ▾

Directions For sunscreen use: apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hours 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

⚠️ Warnings 56 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 product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 14 words ▾

Other information Protect the product in this container from excessive heat and direct sun

🧪 Active Ingredient 15 words ▾

Active ingredients Purpose Avobenzone (3.0%) Sunscreen Homosalate (5.0%) Sunscreen Octisalate (5.0%) Sunscreen Octocrylene (3.0%) Sunscreen

🧪 Inactive Ingredients 60 words ▾

Inactive ingredients Water, Butyloctyl Salicylate, Butylene Glycol, Octyldodecyl Neopentanoate, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Glycerin, Ascophyllum Nodosum Extract, Silica, Ethylhexylglycerin, Cetearyl Alcohol, Coco-Glucoside, Citric Acid, Batyl Alcohol, BIS-PEG/PPG-14/14 Dimethicone, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Disodium EDTA, Potassium Hydroxide, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Xanthan Gum, Saccharide Isomerate, Sodium Citrate, Tin Oxide, Phenoxyethanol, Potassium Sorbate.

May Contain: Iron Oxides, Mica, Titanium Dioxide.

🎯 Purpose 15 words ▾

Active ingredients Purpose Avobenzone (3.0%) Sunscreen Homosalate (5.0%) Sunscreen Octisalate (5.0%) Sunscreen Octocrylene (3.0%) 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 21 words ▾

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

📄 Questions or Comments 14 words ▾

Questions or comments? Call toll free 1-888-637-2437 M – F 9am – 5pm CST

📄 Package Label / Principal Display Panel ~3 min read ▾

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 0N1 Petal LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 0N1 Petal

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 0W1 Pearl LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 0W1 Pearl

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1C0 Cameo LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1C0 Cameo

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1W1 Porcelain LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1W1 Porcelain

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2N1 Nude LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2N1 Nude

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2W1 Natural LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2W1 Natural

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3N1 Sand LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3N1 Sand

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3W1 Bisque LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3W1 Bisque

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4C1 Almond LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4C1 Almond

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4W1 Tawny LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4W1 Tawny

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5N1 Walnut LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5N1 Walnut

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5W1 Tan LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5W1 Tan

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 6N1 Mocha LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 6N1 Mocha

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 6C1 Cacao LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER LIGHT REVEALER Natural Skin Illuminator Broad Spectrum SPF 25 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 6C1 Cacao

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 Avobenzone, homosalate, octisalate, and octocrylene — the ingredient across all brands.

Top reported reactions

Skin Cancer58
Basal Cell Carcinoma21
Neoplasm Malignant21
Rash21
Malignant Melanoma19
Product Lot Number Issue12
Recalled Product Administered11

Age at onset

Infant1
Child2
Adolescent2
Adult42
Elderly19

Reporter sex

259 reports
Male · 33%
Female · 67%

Serious outcomes

Death5
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 193 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.

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 Laura Mercier US Buyer LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Laura Mercier US Buyer LLC 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.
← 82761-0013-60 · Laura 82761-0035-60 · Laura →
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.