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VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen Titanium Dioxide, Octinoxate 1.35 g/100g; 7.5 g/100g Cream — NDC 87489-0002-02 package photo

VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen Titanium Dioxide, Octinoxate 1.35 g/100g; 7.5 g/100g Cream

by LCM TECHNOLOGY Co., Ltd · 1 TUBE in 1 BOX (87489-002-02) / 40 g in 1 TUBE (87489-002-01)
NDC 87489-0002-02
🏷️ FDA NDC (as labeled) 87489-002-02 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) 87489-002-02
Product NDC 87489-002
11-digit billing NDC 87489000202
UNII 15FIX9V2JP, 4Y5P7MUD51
Application # M020
SPL Set ID 4cbbf8aa-8910-b7e7-e063-6294a90a4f07
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-11
Route TOPICAL
Dosage form CREAM
Substance TITANIUM DIOXIDE; ETHYLHEXYL METHOXYCINNAMATE
Why two NDCs? The FDA registers this code as 87489-002-02 — 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 → 87489-0002-02. 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

LabelerLCM TECHNOLOGY Co., Ltd
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87489
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio2 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?

VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen is a topical cream containing two active ingredients commonly used as ultraviolet (UV) light filters in sunscreen products. Titanium dioxide and ethylhexyl methoxycinnamate (also called octinoxate) function as physical and chemical UV blockers, respectively, and are typical components in over-the-counter sun protection formulations. This product is marketed as an OTC monograph drug, meaning it follows FDA's established category rules for sunscreen products rather than undergoing individual product review.

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 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 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 YCD50O0Z6L
    A synthetic oily liquid used as a solvent and conditioning agent in topical formulations. It helps dissolve other ingredients and improves how the product spreads and feels on skin.
  • UNII Z11006CMUZ
    A synthetic sunscreen chemical used as a UV filter in topical formulations. It absorbs ultraviolet light to help protect the product and skin from sun damage.
  • UNII 4X49Y0596W
    Ethylhexyl salicylate is a synthetic organic compound used as a UV filter and penetration enhancer in topical formulations. It helps protect the product and skin from ultraviolet light damage.
  • UNII XQN8R9SAK4
    A synthetic ultraviolet filter compound used in topical formulations to absorb and protect against harmful UV rays. It functions as an active sunscreen agent rather than a traditional inactive filler or binder.
  • 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 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 8NT850T0YS
    A synthetic chemical compound used as an ultraviolet light absorber and antioxidant. It protects the medicine from degradation caused by light and oxygen exposure during storage.
  • 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 XJ7052W897
    A synthetic ester derived from pentaerythritol, used primarily 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 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 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII GW89575KF9
    Squalane is a lightweight oil derived from plant sources or synthesized. It acts as an emollient and lubricant in formulations, helping ingredients blend smoothly and improving product texture and spreadability.
  • UNII 5041RX63GN
    A synthetic silicon-based polymer used as a glidant and anti-caking agent. It helps powder particles flow smoothly and prevents clumping during manufacturing and 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.

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

The official label also statesWater, Ethylhexyl, Methoxycinnamate, Isododecane, Butylene Glycol, Cyclopentasiloxane, Niacinamide, Ethylhexyl, Salicylate, Silica, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Ethylhexyl Triazone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Dimethyl PABA, Bis-Ethylhexyloxypenol Methoxyphenyl Triazine, Potassium Cetyl Phosphate, Sodium Chloride, Diethylhexyl Carbonate, Butyloctyl Sulfate, Trimethylsiloxysilicate, Pentaerythrityl Tetraethylhexanoate, Glycerin, Squalane, Bisabolol, Sodium Chloride, Phenoxyethanol, Polysorbate, Sodium Benzoate.

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
VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen 1.35 g/100g; 7.5 g/100gthis 87489-0002-02 LCM 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

🏛️
2026
On the market since
Mar 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87489-0002-02 You're viewing this 1 TUBE in 1 BOX (87489-002-02) / 40 g in 1 TUBE (87489-002-01) 2026-03-11 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 87489-002-02, 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: 87489-0002-02, written without dashes as 87489000202. 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 87489-0002-02, the first segment (87489) is the labeler code FDA assigned to LCM TECHNOLOGY Co., Ltd; the middle segment (0002) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 LCM TECHNOLOGY Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
LCM TECHNOLOGY 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.

📄 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 33 words ▾

Apply 15 minutes before sun exposure. Reapply at least every 2 hours. Children under 6 months of age: ask a doctor. Apply generously and evenly to face and exposed areas of the body.

⏱️ Dosage and Administration 17 words ▾

Helps prevent sunburn. Decreases the risk of skin cancer and early skin aging caused by the sun.

⚠️ Warnings 109 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 using and consult a doctor if rash or irritation occurs. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and earlyskin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15or 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

🧪 Active Ingredient 8 words ▾

Ethylhexyl Methoxycinnamate (Octinoxate) 7.5% Titanium Dioxide (Nano) 1.35%

🧪 Inactive Ingredients 47 words ▾

Water, Ethylhexyl, Methoxycinnamate, Isododecane, Butylene Glycol, Cyclopentasiloxane, Niacinamide, Ethylhexyl, Salicylate, Silica, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Ethylhexyl Triazone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Dimethyl PABA, Bis-Ethylhexyloxypenol Methoxyphenyl Triazine, Potassium Cetyl Phosphate, Sodium Chloride, Diethylhexyl Carbonate, Butyloctyl Sulfate, Trimethylsiloxysilicate, Pentaerythrityl Tetraethylhexanoate, Glycerin, Squalane, Bisabolol, Sodium Chloride, Phenoxyethanol, Polysorbate, Sodium Benzoate.

🎯 Purpose 1 words ▾

sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87489-0001-02 · LCM 87492-0001-01 · Shenzhen →
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.