Home › NDC Lookup › Ingredients › Octinoxate, Titanium Dioxide, Zinc Oxide › 68577-0188-00
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg Cream, 30 mg — NDC 68577-0188-00 package photo

Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg Cream, 30 mg

by COSMAX USA, INC · 30 mg in 1 BOTTLE, GLASS (68577-188-00)
NDC 68577-0188-00
🏷️ FDA NDC (as labeled) 68577-188-00 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 68577-188-00
Product NDC 68577-188
11-digit billing NDC 68577018800
UNII SOI2LOH54Z, 15FIX9V2JP, 4Y5P7MUD51
Application # M020
SPL Set ID 29abdf3c-fb54-a5e3-e063-6394a90af450
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-02-15
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE
Why two NDCs? The FDA registers this code as 68577-188-00 — 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 → 68577-0188-00. 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

LabelerCOSMAX USA, INC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code68577
First marketedFeb 2018
Product typeHuman Otc Drug
Portfolio15 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?

Light Illusion Luminous Makeup Nude-Skin Feel SPF18 is an over-the-counter topical cream makeup product marketed under FDA's sunscreen monograph rules. It contains three active sunscreen ingredients: octinoxate and titanium dioxide, which are ultraviolet light filters, and zinc oxide, which functions as both a UV filter and a physical barrier. These ingredients are typically used together in sunscreen products to help protect skin from sun exposure. This product is formulated as a cream applied directly to the 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.

🧪 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 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • 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 75D21FL1PI
    A synthetic liquid derived from butylene glycol and fatty acids. It acts as an emollient and solvent to help dissolve or suspend active ingredients, improving texture and absorption in topical or oral formulations.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII G300307ZXP
    A silicone-based emulsifier made from cetyl alcohol and polydimethylsiloxane. It helps mix oil and water components in creams and lotions, and improves product texture and spreadability.
  • 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 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 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • 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 G7036X8B5H
    A dark iron compound that gives medicine its color. Used as a colorant in tablets and capsules to help identify the medication 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 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 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 U68ZV6W62C
    A synthetic oily substance used as a solvent and emollient in topical medicines. It helps dissolve active ingredients and improves how the product spreads on skin.
  • UNII 8PR7V1SVM0
    A silicone-based lubricant combined with polyethylene glycol. It reduces friction and helps the medicine flow smoothly during manufacturing and improves how the product feels when applied or swallowed.
  • 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 Z47NNT4J11
    A synthetic plastic polymer used as a film-coating material on tablets and capsules. It helps protect the medicine, control how fast it dissolves, and improve appearance by creating a smooth, glossy outer layer.
  • UNII 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • UNII OLX698AH5P
    A clay mineral processed with a quaternary ammonium compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • 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 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.

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

The official label also statesInactive ingredients: Water, Ethylhexyl Palmitate, Butylene Glycol, Caprylic/Capric Triglyceride, Butylene Glycol Dicaprylate/Dicaprate, Glycerin, Neopentyl Glycol Diethylhexanoate, Cetyl Ethylhexanoate, PEG-30 Dipolyhydroxystearate, Pentylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Polymethyl Methacrylate, PEG-10 Dimethicone, Cyclopentasiloxane, Phenoxyethanol, Magnesium Sulfate, Sorbitan Isostearate, Beeswax, Stearalkonium Hectorite, Triethoxycaprylylsilane, Aluminum Hydroxide, Stearic Acid, Dimethicone, Ethylhexylglycerin, Disodium EDTA. May Contain: Titanium Dioxide, Iron Oxides, Mica.

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 IVORY 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0176-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mgthis 68577-0188-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CLASSIC TAN 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0181-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 MOCHA 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0186-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 TAWNY 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0182-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18- D2 NUTMEG 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0185-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 WARM BEIGE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0178-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SHELL 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0174-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 PORCELAIN 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0175-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SOFT SAND 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0180-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 COCOA 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0187-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 NUDE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0177-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CARAMEL 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0183-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SABLE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0184-00 COSMAX 30 mg — — FDA listed —
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 NATURAL BEIGE 4.9 mg/100mg; 2 mg/100mg; 5 mg/100mg 68577-0179-00 COSMAX 30 mg — — 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

🏛️
2018
On the market since
Feb 2018
📍
2026
Currently FDA-listed
8 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
68577-0188-00 You're viewing this 30 mg in 1 BOTTLE, GLASS (68577-188-00) 2018-02-15 Active

🧭 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 68577-188-00, 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: 68577-0188-00, written without dashes as 68577018800. 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 68577-0188-00, the first segment (68577) is the labeler code FDA assigned to COSMAX USA, INC; the middle segment (0188) 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 COSMAX USA, INC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
COSMAX USA, INC 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 32 words ▾

USES 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 Drections For sunscreen use: Apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months of age: Ask a doctor

⚠️ Warnings 57 words ▾

WARNINGS 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.

🧪 Active Ingredient 10 words ▾

Active Ingredients Octinoxate 5% Titanium Dioxide 2% Zinc Oxide 4.9%

🧪 Inactive Ingredients 54 words ▾

Inactive ingredients: Water, Ethylhexyl Palmitate, Butylene Glycol, Caprylic/Capric Triglyceride, Butylene Glycol Dicaprylate/Dicaprate, Glycerin, Neopentyl Glycol Diethylhexanoate, Cetyl Ethylhexanoate, PEG-30 Dipolyhydroxystearate, Pentylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Polymethyl Methacrylate, PEG-10 Dimethicone, Cyclopentasiloxane, Phenoxyethanol, Magnesium Sulfate, Sorbitan Isostearate, Beeswax, Stearalkonium Hectorite, Triethoxycaprylylsilane, Aluminum Hydroxide, Stearic Acid, Dimethicone, Ethylhexylglycerin, Disodium EDTA.

May Contain: Titanium Dioxide, Iron Oxides, Mica.

🎯 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 ↗
← 68577-0187-00 · COSMAX 68577-0189-00 · COSMAX →
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.