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LUXE COLOR FOUNDATION Octinoxate 7% Zinc Oxide 5% .07 mg/30mL; .05 mg/30mL Emulsion, 30 mL — NDC 87204-0248-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

LUXE COLOR FOUNDATION Octinoxate 7% Zinc Oxide 5% .07 mg/30mL; .05 mg/30mL Emulsion, 30 mL — NDC 87204-248-01 (Billing 87204-0248-01)

by Guangzhou Huixue Biotechnology Co., Ltd. · 30 mL in 1 BOX, UNIT-DOSE

This is a package of 30 mL of LUXE COLOR FOUNDATION Octinoxate 7% Zinc Oxide 5% .07 mg/30mL; .05 mg/30mL Emulsion from Guangzhou Huixue Biotechnology Co., Ltd., marketed since Jul 2026 and currently FDA-listed, this package's marketing is listed to end Jul 2027. It is this product's only package size.

NDC 87204-0248-01
🏷️ FDA NDC (as labeled) 87204-248-01 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 Jul 30, 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 87204-248-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87204 labeler · 248 product · 01 package
Package marketed since
Jul 15, 2026
Package marketing ended
Jul 20, 2027
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 8720424801 9
FDA record last changed
Jul 30, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87204-248-01
Product NDC 87204-248
11-digit billing NDC 87204024801
UNII 4Y5P7MUD51, SOI2LOH54Z
Application # M020
SPL Set ID 576c3496-702f-808c-e063-6394a90a53c3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-15
Marketing end 2027-07-20
Route TOPICAL
Dosage form EMULSION
Substance OCTINOXATE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 87204-248-01 — 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 → 87204-0248-01. 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?

Luxe Color Foundation is a topical emulsion (liquid makeup) containing two sunscreen active ingredients: octinoxate and zinc oxide. These ingredients are commonly used together in sunscreen products to filter and block ultraviolet (UV) light from the sun. This product is marketed as an over-the-counter monograph drug, meaning it follows the FDA's established rules for sunscreen formulations rather than being individually reviewed. The emulsion base allows the sunscreen ingredients to be blended into a foundation product for application to facial skin.

Supplement & herbal interactions

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

Pricing

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

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
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
87204-0248-01 You're viewing this Main listing 30 mL in 1 BOX, UNIT-DOSE 2026-07-15 Jul 20, 2027 Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Luxe Color Foundation .07 mg/30mL; .05 mg/30mLthis 87204-0248-01 Guangzhou 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

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

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

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

Inactive Ingredients / Excipients

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

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

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 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 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 CI87N1IM01
    A mixture of liquid hydrocarbons derived from petroleum, used as a lubricant and glidant to help the medicine flow smoothly during manufacturing and ensure even tablet coating or capsule filling.
  • 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 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII F4K100DXP3
    Dibutyl adipate is a synthetic oily liquid derived from adipic acid. It serves as a plasticizer and solvent in medicines, helping softens coatings and improves flexibility so tablets and capsules don't crack or break.
  • 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 UF7620L1W6
    A synthetic silicone polymer that acts as a thickener and absorbent in medicines. It helps create the right texture, improves how the product feels on skin or in the mouth, and can absorb excess moisture or oil in formulations.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 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 Y6O7T4G8P9
    Hydrated silica is a fine powder form of silicon dioxide with absorbed water. It works as an anti-caking agent and absorbent in medicines, helping powders stay free-flowing and preventing clumping.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 25KRT26H77
    A synthetic organic compound used as a preservative and antioxidant in medicines. It helps prevent breakdown and spoilage of the active ingredients during storage.
  • 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 S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII 9713Q0S7FO
    A synthetic emulsifier derived from polyethylene glycol and fatty acids. It helps blend water and oil-based ingredients together in the formulation, improving texture and stability.
  • 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 9YQ9DI1W42
    A chemical compound used as a UV filter in topical formulations. It absorbs ultraviolet light to help protect the product and its active ingredients from degradation during storage and use.
  • UNII 7F465U79Q1
    A clay mineral treated with a quaternary ammonium compound to make it water-soluble. Used as a thickener, suspending agent, and stabilizer to give products a smooth texture and prevent separation of ingredients.
  • UNII EU2PSP0G0W
    Silica dimethyl silylate is a silicon-based powder that acts as a glidant and anti-caking agent. It reduces friction between particles and helps powders flow smoothly during manufacturing and tablet compression.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • 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 LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • 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.

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

The official label also statesWATER, BUTYLENE GLYCOL,C15-19 ALKANE, DIBUTYL ADIPATE, CYCLOPENTASILOXANE,ISONONYL ISONONANOATE, BIFIDA FERMENT FILTRATE, PHENYLBENZIMIDAZOLE SULFONIC ACID, SILICA, PEG-30 DIPOLYHYDROXYSTEARATE, TRIMETHYLSILOXYSILICATE, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, GALACTOMYCES FERMENT FILTRATE, QUATERNIUM-18 BENTONITE, ISODODECANE,PHENOXYETHANOL, BISABOLOL, MAGNESIUM SULFATE, PEG-10 DIMETHICONE, POLYHYDROXYSTEARIC ACID, PORTULACA OLERACEA EXTRACT, DIMETHICONE CROSSPOLYMER, CI 77492, SODIUM HYDROXIDE, ALUMINUM HYDROXIDE, HYDRATED SILICA, TRIETHOXYCAPRYLYLSILANE, DIMETHICONE, CI 77491, SILICA DIMETHYL SILYLATE, DISTEARDIMONIUM HECTORITE, GLYCERIN, 1,2-HEXANEDIOL, TOCOPHEROL,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HYDROXYACETOPHENONE, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, PHYLLANTHUS EMBLICA FRUIT EXTRACT, ROSA ROXBURGHII FRUIT EXTRACT, SOPHORA FLAVESCENS ROOT EXTRACT, TRIBULUS TERRESTRIS FRUIT EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT.

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

LabelerGuangzhou Huixue Biotechnology Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87204
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio46 products on file

More NDCs from Guangzhou Huixue Biotechnology Co., Ltd. labeler code 87204

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

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 56 words ▾

Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) decreases the risk of skin cancer and early skin aging caused by the sun.Directions Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water-resistant sunscreen if Swimming or Sweating Children under 6 months: ask c doctor

⏱️ Dosage and Administration 36 words ▾

Apply evenly to clean skin before sun exposure. Massage in a circular motion with your fingers until the shade blends with your skin tone. Lightweight and breathable, it offers long-lasting wear for a flawless, natural finish.

⚠️ Warnings 52 words ▾

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 immediately

🧪 Active Ingredient 5 words ▾

Octinoxate 7% Zinc Oxide 5%

🧪 Inactive Ingredients 86 words ▾

WATER, BUTYLENE GLYCOL,C15-19 ALKANE, DIBUTYL ADIPATE, CYCLOPENTASILOXANE,ISONONYL ISONONANOATE, BIFIDA FERMENT FILTRATE, PHENYLBENZIMIDAZOLE SULFONIC ACID, SILICA, PEG-30 DIPOLYHYDROXYSTEARATE, TRIMETHYLSILOXYSILICATE, POLYMETHYLSILSESQUIOXANE, NIACINAMIDE, GALACTOMYCES FERMENT FILTRATE, QUATERNIUM-18 BENTONITE, ISODODECANE,PHENOXYETHANOL, BISABOLOL, MAGNESIUM SULFATE, PEG-10 DIMETHICONE, POLYHYDROXYSTEARIC ACID, PORTULACA OLERACEA EXTRACT, DIMETHICONE CROSSPOLYMER, CI 77492, SODIUM HYDROXIDE, ALUMINUM HYDROXIDE, HYDRATED SILICA, TRIETHOXYCAPRYLYLSILANE, DIMETHICONE, CI 77491, SILICA DIMETHYL SILYLATE, DISTEARDIMONIUM HECTORITE, GLYCERIN, 1,2-HEXANEDIOL, TOCOPHEROL,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HYDROXYACETOPHENONE, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, PHYLLANTHUS EMBLICA FRUIT EXTRACT, ROSA ROXBURGHII FRUIT EXTRACT, SOPHORA FLAVESCENS ROOT EXTRACT, TRIBULUS TERRESTRIS FRUIT EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT.

🎯 Purpose 28 words ▾

Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) decreases the risk of skin cancer and early skin aging caused by the sun.

📄 Do Not Use 14 words ▾

Do not use on damaged on broken skin，Children under 6 months: ask a doctor

📄 When Using This Product 28 words ▾

Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water-resistant sunscreen If swimming or sweating Children under 6 months ask a docton

📄 Keep Out of Reach of Children 13 words ▾

Protect this product from excessive heat and direct sun Store at 15-30°℃ (59-86°F)

📄 Package Label / Principal Display Panel 6 words ▾

LUXE COLOR FOUNDATION LUXE COLOR FOUNDATION

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

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 it is currently marketed — but Guangzhou Huixue Biotechnology Co., Ltd. has reported a marketing end date of 2027-07-20, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Huixue Biotechnology Co., Ltd. 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.
← 87204-0212-01 · Guangzhou 87204-0285-01 · Guangzhou →
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.