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Dr Marvel COLOR CHANGING FOUNDATION SPF30 ETHYLHEXYL METHOXYCINNAMATE 2 mg/100mg; 2 mg/100mg; 4.995 mg/100mg Cream, 50 mg

by Guangzhou Liyan Cosmetics Technology Co., Ltd. · 50 mg in 1 BOX (87770-013-01)
NDC 87770-0013-01
🏷️ FDA NDC (as labeled) 87770-013-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 3, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

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Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 87770-013-01
Product NDC 87770-013
11-digit billing NDC 87770001301
UNII 4X49Y0596W, 5A68WGF6WM, 4Y5P7MUD51
Application # M020
SPL Set ID 59c8865f-ccee-dd50-e063-6294a90aa185
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-24
Route TOPICAL
Dosage form CREAM
Substance ETHYLHEXYL SALICYLATE; OCTOCRYLENE; ETHYLHEXYL METHOXYCINNAMATE
Why two NDCs? The FDA registers this code as 87770-013-01 — 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 → 87770-0013-01. 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.

🏭 Manufacturer & labeler

LabelerGuangzhou Liyan Cosmetics Technology Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87770
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio8 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?

Dr Marvel Color Changing Foundation SPF30 is a topical cream formulated as an over-the-counter sunscreen product under FDA monograph standards. It contains three active UV filter ingredients: ethylhexyl methoxycinnamate, ethylhexyl salicylate, and octocrylene, which are commonly used together to absorb ultraviolet radiation and help protect skin from sun damage. This type of product is typically applied to the face and body to provide broad-spectrum sun protection with an SPF rating of 30.

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.

💊 What it looks like

ShapeRectangle
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

  • 50.69322 mg / 100 mg 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesAQUA BUTYLENE GLYCOL CI 77891 ISOHEXADECANE C12-15 ALKYL BENZOATE CETYL PEG/PPG-10/1 DIMETHICONE GLYCERIN TRIMETHYLSILOXYSILICATE MICA DIMETHICONE CYCLOPENTASILOXANE SODIUM CHLORIDE PANTHENOL DIISOSTEARYL MALATE MAGNESIUM STEARATE PHENOXYETHANOL DISTEARDIMONIUM HECTORITE CI 77492 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER TRIETHOXYCAPRYLYLSILANE SQUALANE CI 77491 ALUMINUM HYDROXIDE ETHYLHEXYLGLYCERIN CI 77499 POLYVINYL ALCOHOL 1,2-HEXANEDIOL TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT SODIUM POLYACRYLATE OPUNTIA DILLENII EXTRECT AVENA SATIVA (OAT) EXTRACT BHT FUCUS VESICULOSUS EXTRACT ASTRAGALUS MEMBRANACEUS EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT ATRACTYLODES MACROCEPHALA ROOT EXTRACT SAPOSHNIKOVIA DIVARICATA ROOT EXTRACT HIBISCUS ABELMOSCHUS EXTRACT GLYCYRRHIZA INFLATA EXTRACT CENTELLA ASIATICA 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.

💲 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
Dr Marvel COLOR CHANGING FOUNDATION SPF30 2 mg/100mg; 2 mg/100mg; 4.995 mg/100mgthis 87770-0013-01 Guangzhou 50 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

🏛️
2026
On the market since
Aug 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
87770-0013-01 You're viewing this 50 mg in 1 BOX (87770-013-01) 2026-08-24 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 — Not published for this NDC No photo available yet for this listing.
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 87770-013-01, 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: 87770-0013-01, written without dashes as 87770001301. 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 87770-0013-01, the first segment (87770) is the labeler code FDA assigned to Guangzhou Liyan Cosmetics Technology Co., Ltd.; the middle segment (0013) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Guangzhou Liyan Cosmetics Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Liyan Cosmetics 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 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 31 words ▾

Indications & Usage • Helps prevent sunburn. • If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 37 words ▾

Directions • Adults and children 6 months of age and older: Apply generously and evenly 15 minutes before sun exposure. • Reapply at least every 2 hours. • Children under 6 months of age: Ask a doctor.

⚠️ Warnings 95 words ▾

Warnings • Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product helps prevent sunburn; it does not reduce the risk of skin cancer or early skin aging. • For external use only. • Do not use on broken or damaged skin. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • Stop use and consult a doctor if skin rash develops. • Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Inactive Ingredients 85 words ▾

AQUA BUTYLENE GLYCOL CI 77891 ISOHEXADECANE C12-15 ALKYL BENZOATE CETYL PEG/PPG-10/1 DIMETHICONE GLYCERIN TRIMETHYLSILOXYSILICATE MICA DIMETHICONE CYCLOPENTASILOXANE SODIUM CHLORIDE PANTHENOL DIISOSTEARYL MALATE MAGNESIUM STEARATE PHENOXYETHANOL DISTEARDIMONIUM HECTORITE CI 77492 DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER TRIETHOXYCAPRYLYLSILANE SQUALANE CI 77491 ALUMINUM HYDROXIDE ETHYLHEXYLGLYCERIN CI 77499 POLYVINYL ALCOHOL 1,2-HEXANEDIOL TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT SODIUM POLYACRYLATE OPUNTIA DILLENII EXTRECT AVENA SATIVA (OAT) EXTRACT BHT FUCUS VESICULOSUS EXTRACT ASTRAGALUS MEMBRANACEUS EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT ATRACTYLODES MACROCEPHALA ROOT EXTRACT SAPOSHNIKOVIA DIVARICATA ROOT EXTRACT HIBISCUS ABELMOSCHUS EXTRACT GLYCYRRHIZA INFLATA EXTRACT CENTELLA ASIATICA EXTRACT

🎯 Purpose 19 words ▾

Evens out skin texture, conceals dullness, brightens complexion, gently protects against UV rays, and creates a natural, seamless base.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87770-0006-01 · Guangzhou 87770-0025-01 · 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.