Home › NDC Lookup › Ingredients › Avobenzone, Octinoxate, Octocrylene, And... › 82761-0042-60
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0W1 Pearl AVOBENZONE, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL Cream — NDC 82761-0042-60 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 Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0W1 Pearl AVOBENZONE, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL Cream — NDC 82761-042-60 (Billing 82761-0042-60)

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 Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0W1 Pearl AVOBENZONE, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL Cream from Laura Mercier US Buyer LLC, marketed since Aug 2022 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 82761-0042-60
🏷️ FDA NDC (as labeled) 82761-042-60 billing pads the product segment with a zero
This package
Contains50 mL in 1 tube Pack sizes2 compare ↓
Main listing for product 82761-042 · Also comes in: 25 mL 82761-042-61
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82761-042-60
Product NDC 82761-042
11-digit billing NDC 82761004260
UNII G63QQF2NOX, 5A68WGF6WM, 95OOS7VE0Y, 4Y5P7MUD51
Application # M020
SPL Set ID e78f9689-2f8b-1524-e053-2995a90adc79
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; OCTINOXATE; OCTOCRYLENE; OXYBENZONE
Why two NDCs? The FDA registers this code as 82761-042-60 — 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 → 82761-0042-60. 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 topical cream marketed as a tinted moisturizer with broad spectrum sun protection. It contains four active ingredients that function as ultraviolet (UV) filters: avobenzone, octinoxate, octocrylene, and oxybenzone. These are commonly used together in sunscreen products to help absorb and scatter UVA and UVB rays. The product is an over-the-counter monograph drug, meaning it follows FDA's established rules for sunscreen products rather than being individually approved through a separate application.

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.
Try another pack size: 25 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
82761-0042-60 You're viewing this Main listing 1 TUBE in 1 CARTON / 50 mL in 1 TUBE 2022-08-31 — Active
82761-0042-61 82761-042-61 1 TUBE in 1 CARTON / 25 mL in 1 TUBE 2022-08-31 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 carton / 50 ml in 1 tube.
What NDC number is used to bill for this package of Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0W1 Pearl AVOBENZONE, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL Cream?
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
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0N1 Petal 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0035-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 1N2 Vanille 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0036-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 2N1 Nude 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0037-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 3N1 Sand 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0038-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 4W1 Tawny 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0039-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 5W1 Tan 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0040-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 0W1 Pearl 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mLthis 82761-0042-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 1W1 Porcelain 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0043-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 2W1 Natural 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0044-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 4C1 Almond 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0045-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 5C1 Nutmeg 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0046-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 6C1 Cacao 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0047-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 3W1 Bisque 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0048-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 1C0 Cameo 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0049-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 2C1 Blush 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0050-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 3C1 Fawn 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0051-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 4N1 Wheat 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0052-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 5N1 Walnut 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0053-60 Laura 1 tube — — FDA listed —
Laura Mercier Tinted Moisturizer Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 6W1 Ganache 1.25 g/50mL; 3.745 g/50mL; 1 g/50mL; .5 g/50mL 82761-0054-60 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 H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII Q7UI015FF9
    A synthetic polymer material used as a thickener and stabilizer in liquid formulations. It helps create the right texture and prevents separation of ingredients in medicines and topical products.
  • 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 H390488X0A
    Behenic acid is a waxy substance derived from plant oils. It functions as a lubricant and binder in tablets and capsules, helping reduce friction during manufacturing and holding ingredients together.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • 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 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • 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 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 9E4CO0W6C5
    A silicone-based polymer that forms soft, spongy particles. Used as a texture modifier and suspending agent to improve how the product feels and flows, and to help keep ingredients evenly distributed throughout the formulation.
  • UNII 9G1OE216XY
    Docosanol is a waxy, fatty alcohol derived from plant sources. It acts as an emollient and thickener in topical medicines, helping to soften the skin and improve product texture and stability.
  • 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 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 U333RI6EB7
    Hydrogenated polydecene type I is a synthetic oil derived from plant-based polymers. It acts as a lubricant and glidant to help powder ingredients flow smoothly during tablet or capsule manufacturing.
  • 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 TP11QR7B8R
    A natural oil extracted from kukui nuts, used as an emollient and skin-conditioning agent in topical medicines. It helps soften the formulation and improve how the product spreads and absorbs into skin.
  • UNII 515610SU8C
    Macadamia oil is a plant-derived oil extracted from macadamia nuts. In medicines, it serves as an emollient and solvent to help dissolve or suspend active ingredients and improve product texture and absorption.
  • UNII 8CAC4NQ872
    A synthetic emulsifier made from polyethylene glycol and stearic acid. It helps mix oil and water-based ingredients together and improves the product's texture and stability in creams, lotions, and other formulations.
  • UNII 6DNW9T7YT2
    A synthetic liquid polymer made from ethylene and propylene compounds. It acts as a solvent and humectant to help dissolve active ingredients and maintain moisture in the formulation.
  • 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 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 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 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 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 K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly 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 P1BM4ZH95L
    A salt derived from phosphoric acid, sodium polymetaphosphate acts as a sequestrant and buffering agent in medicines. It helps maintain stability and control acidity in liquid formulations.
  • 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 MD83SFE959
    A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
  • 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 6RG2461FCH
    A natural plant-based wax derived from the fruit rind of Toxicodendron vernicifluum (Chinese lacquer tree). Used as a coating agent and lubricant to provide a smooth surface on tablets or capsules and improve handling during manufacturing.
  • UNII B8WCK70T7I
    Trehalose is a natural sugar made from two glucose molecules linked together. It's used in medicines as a filler to add bulk, a sweetener for taste, and a stabilizer to help keep active ingredients effective during storage.
  • 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.

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

The official label also statesWATER, GLYCERIN, BUTYLENE GLYCOL, DIMETHICONE, PEG/PPG-14/7 DIMETHYL ETHER, HYDROGENATED POLYDECENE, PEG-5 GLYCERYL STEARATE, ISODODECANE, SILICA, PHENYL TRIMETHICONE, TREHALOSE, PHENOXYETHANOL, TOCOPHEROL, BUTYROSPERMUM PARKII (SHEA) BUTTER, MACADAMIA TERNIFOLIA SEED OIL, ALEURITES MOLUCCANUS SEED OIL, RHUS VERNICIFLUA PEEL WAX, TAMARINDUS INDICA SEED GUM, SACCHARIDE ISOMERATE, PENTYLENE GLYCOL, ISOSTEARIC ACID, GLYCERYL STEARATE SE, POLYSILICONE-11, BEHENYL ALCOHOL, BEHENIC ACID, STEARIC ACID, BATYL ALCOHOL, HYDROXYPROPYL METHYLCELLULOSE STEAROXY ETHER, PEG-30 PHYTOSTEROL, DISODIUM EDTA, SODIUM METAPHOSPHATE, CARBOMER, POLYACRYLATE CROSSPOLYMER-6, POTASSIUM HYDROXIDE, BHT, SODIUM CITRATE, CITRIC ACID, T-BUTYL ALCOHOL. MAY CONTAIN: TITANIUM DIOXIDE, IRON OXIDES.

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
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. Very long sections are excerpted here and marked; the full text is on DailyMed (linked in the sources below). 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 95 words ▾

Directions For sunscreen use: apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen 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 Reapply at least every 2 hours Use a water-resistant sunscreen if swimming or sweating

⚠️ 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 10 words ▾

Active ingredients AVOBENZONE 2.5% OCTINOXATE 7.49% OCTOCRYLENE 2.0% OXYBENZONE 1.0%

🧪 Inactive Ingredients 88 words ▾

Inactive ingredients WATER, GLYCERIN, BUTYLENE GLYCOL, DIMETHICONE, PEG/PPG-14/7 DIMETHYL ETHER, HYDROGENATED POLYDECENE, PEG-5 GLYCERYL STEARATE, ISODODECANE, SILICA, PHENYL TRIMETHICONE, TREHALOSE, PHENOXYETHANOL, TOCOPHEROL, BUTYROSPERMUM PARKII (SHEA) BUTTER, MACADAMIA TERNIFOLIA SEED OIL, ALEURITES MOLUCCANUS SEED OIL, RHUS VERNICIFLUA PEEL WAX, TAMARINDUS INDICA SEED GUM, SACCHARIDE ISOMERATE, PENTYLENE GLYCOL, ISOSTEARIC ACID, GLYCERYL STEARATE SE, POLYSILICONE-11, BEHENYL ALCOHOL, BEHENIC ACID, STEARIC ACID, BATYL ALCOHOL, HYDROXYPROPYL METHYLCELLULOSE STEAROXY ETHER, PEG-30 PHYTOSTEROL, DISODIUM EDTA, SODIUM METAPHOSPHATE, CARBOMER, POLYACRYLATE CROSSPOLYMER-6, POTASSIUM HYDROXIDE, BHT, SODIUM CITRATE, CITRIC ACID, T-BUTYL ALCOHOL.

MAY CONTAIN: TITANIUM DIOXIDE, IRON OXIDES.

🎯 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 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 ~4 min read ▾

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 0N1 - Petal LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 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 Natural Skin Perfector Broad Spectrum SPF 30 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 Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 1C0 - Cameo

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1N2 - Vanille LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 1N2 - Vanille

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 1W1 - Porcelain LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 1W1 - Porcelain

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2C1 - Blush LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 2C1 - Blush

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 2N1 - Nude LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 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 Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 2W1 - Natural

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3C1 - Fawn LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 3C1 Fawn-

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 3N1 - Sand LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 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 Natural Skin Perfector Broad Spectrum SPF 30 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 Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 4C1 - Almond

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4N1 - Wheat LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 4N1 - Wheat

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 4W1 - Tawny LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 4W1 - Tawny

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5C1 - Nutmeg LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton - 5C1 - Nutmeg

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton - 5N1 - Walnut LAURA MERCIER PARIS | NEW YORK TINTED MOISTURIZER Natural Skin Perfector Broad Spectrum SPF 30 Sunscreen 50 mL /

1.7FL. OZ. LIQ. US Principal Display Panel - 50 mL Tube Carton… [Excerpted — this section continues on DailyMed.]

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, OCTINOXATE, OCTOCRYLENE, and OXYBENZONE — the ingredient across all brands.

Top reported reactions

Rash1
Rash Erythematous1
Rash Pruritic1
Urticaria1

Reporter sex

0 reports
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 1 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 tube (82761-0042-61). 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?
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.
← 82761-0041-60 · Laura 82761-0043-60 · 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.