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EADEM SUNSUEDE DAILY SUNSCREEN AND BLURRING PRIMER SPF50 PLUS Avobenzone, Homosalate, Octisalate, Octocrylene 2.8 g/100g; 6.5 g/100g; 4.5 g/100g; 6.5 g/100g Stick — NDC 87486-0100-01 package photo

EADEM SUNSUEDE DAILY SUNSCREEN AND BLURRING PRIMER SPF50 PLUS Avobenzone, Homosalate, Octisalate, Octocrylene 2.8 g/100g; 6.5 g/100g; 4.5 g/100g; 6.5 g/100g Stick

by EADEM, Inc. · 1 BOTTLE, PLASTIC in 1 CARTON (87486-100-01) / 20 g in 1 BOTTLE, PLASTIC (87486-100-02)
NDC 87486-0100-01
🏷️ FDA NDC (as labeled) 87486-100-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 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) 87486-100-01
Product NDC 87486-100
11-digit billing NDC 87486010001
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM
UPC 0850046839573
Application # M020
SPL Set ID 4ca05e2f-f0c5-821c-e063-6294a90a90b8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-02
Route CUTANEOUS
Dosage form STICK
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 87486-100-01 — 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 → 87486-0100-01. 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

LabelerEADEM, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87486
First marketedApr 2026
Product typeHuman Otc Drug
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?

This is a stick-form sunscreen and primer product applied to the skin, marketed as an over-the-counter monograph drug. It contains four active ingredients: avobenzone, homosalate, octisalate, and octocrylene, which are all ultraviolet (UV) filters commonly used in sunscreens to help protect skin from sun exposure. The product is formulated to function both as a sun protective agent and as a cosmetic primer base.

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 I9PJ0O6294
    A modified starch derived from corn or potato starch with aluminum salt and octenylsuccinic acid added. It acts as a binder to hold tablet ingredients together and as a thickening agent in liquid formulations.
  • UNII 2A88ZO081O
    Pineapple is a tropical fruit extract used as a natural flavoring and coloring agent in medicines. It adds taste and appearance appeal to oral tablets and liquid formulations.
  • UNII 4AJZ4765R9
    A flavoring agent derived from bananas that gives medicine a banana taste. It's added to make oral medications more palatable, especially for children.
  • UNII G27BTQ95MJ
    A plant-derived waxy compound made from oils and alcohols. It acts as an emulsifier and texture agent, helping blend water and oil components together and giving the medicine a smooth, stable consistency.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII U37N0S910T
    A natural oil extracted from camellia seeds, used as an emollient and conditioning agent. It helps soften the product texture and improve skin feel in topical 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 KU94FIY6JB
    A natural enzyme extract from papaya fruit that helps break down proteins. It's used in some medicines as a digestive aid ingredient and may help tablets dissolve or break apart in the stomach.
  • 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 587Z76E9M5
    A chemical compound used as an emulsifier and solubilizer in medications. It helps mix oil and water-based ingredients together and improves how the body absorbs certain drug compounds in the formulation.
  • UNII MCU2324216
    A silicone-based oil that reduces foaming and helps ingredients mix evenly. It's used as an antifoaming agent and lubricant in tablets, capsules, and liquid formulations.
  • 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 H895X08VNQ
    A silicone-based polymer that forms small, hard particles. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII I445L28B12
    A silicone-based compound that acts as a lubricant and glidant in tablet and capsule formulations. It reduces friction between particles and on equipment surfaces, helping medicines flow smoothly during manufacturing and tablet compression.
  • UNII I6KB4GE3K4
    A synthetic oil derived from petrochemicals, used as an emollient and solvent in topical formulations. It helps dissolve active ingredients and improve the texture and spreadability of creams, lotions, and ointments.
  • UNII J9EQA3S2JM
    FD&C Blue No. 1 Aluminum Lake is a blue colorant made by combining FD&C Blue No. 1 dye with aluminum salts. It is used to color tablets, capsules, and other medicines for easy identification and appearance.
  • UNII JQ6BLH9FR7
    FD&C Yellow No. 5 Aluminum Lake is a bright yellow colorant made by combining a synthetic dye with aluminum and other salts. It colors tablets and capsules to help identify the medication and make it visually distinctive.
  • UNII 1340BFH77T
    A plant extract from the mangosteen fruit rind, used as a natural coloring agent or flavoring ingredient in medicines. It may also contribute antioxidant properties to help preserve product stability.
  • UNII 6T0W75Q603
    Guava juice is a liquid derived from guava fruit. In medicines, it functions as a flavoring agent to improve taste and make the product more palatable for patients.
  • UNII AR294KAG3T
    Isoeicosane is a synthetic hydrocarbon liquid used as a solvent and vehicle in medicines. It helps dissolve or suspend active ingredients and improves product stability and texture.
  • UNII 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII 24H4NWX5CO
    Kaolin is a naturally occurring clay mineral. It's used in tablets and capsules as a filler and absorbent to add bulk, improve texture, and help bind ingredients together.
  • UNII J245LN42AI
    Low density polyethylene is a plastic polymer used in medicines as a coating or film-forming agent. It helps protect the active ingredient and controls how fast the medicine dissolves or releases in the body.
  • UNII I629I3NR86
    A natural flavoring derived from mango fruit, used to add taste and aroma to medicines. It helps mask bitter or unpleasant flavors, making the medication more pleasant to take.
  • UNII 7UOL7P5FF5
    A plant extract from the noni tree leaves used as a natural flavoring agent and to add color to the medicine. It may also help preserve the product's stability.
  • UNII 2J089U1OXI
    A natural extract from rambutan fruit, used as a flavoring and coloring agent in medicines to improve taste and appearance.
  • 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 68DUY2D39A
    A waxy emulsifier derived from glycerin and isostearic acid. It helps blend oil and water-based ingredients together and provides texture and consistency in topical formulations.
  • UNII Z570VEV8XK
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles so the medicine flows smoothly during manufacturing and remains free-flowing in the bottle.
  • UNII Q369O8926L
    Resveratrol is a plant-derived compound sometimes added to supplements and fortified products. It may serve as an active nutritional ingredient rather than a traditional inactive filler, though its exact formulation role varies by product.
  • 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 Q3Z4BCH099
    A manufactured wax made from refined petroleum or plant oils. It coats tablet surfaces to control how fast the medicine dissolves and releases, and improves how the tablet feels and looks.
  • UNII Y3NG9WF08W
    Zeolite A is a microporous mineral powder that acts as a drying agent and absorbent in medicines. It removes moisture to keep solid formulations dry and stable during storage.
  • UNII C32PQ86DH4
    Zinc PCA is a zinc salt of pyroglutamic acid, a naturally occurring amino acid derivative. It's used in medications as a skin-conditioning agent and to help maintain product stability and texture in topical formulations.

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

The official label also statesInactive ingredients diethylhexyl carbonate, dimethicone, synthetic wax, methyl methacrylate crosspolymer, butyloctyl salicylate, diphenylsiloxy phenyl trimethicone, C12-15 alkyl benzoate, isopropyl palmitate, diisostearyl malate, ethylhexyl isononanoate, isoeicosane, polyethylene, polymethylsilesquioxane, ethylene/propylene copolymer, dimethicone/vinyl dimethicone crosspolymer, camellia japonica seed oil, bis-behenyl/isostearyl/phytosteryl dimer dilinoleyl dimer dilinoleate, ananas sativus (pineapple) fruit extract, carica papaya (papaya) fruit extract, garcinia mangostana peel extract, mangifera indica (mango) fruit extract, morinda citrifolia extract, musa sapientum (banana) fruit extract, nephelium lappaceum branch/fruit/leaf extract, psidium guajava fruit extract, resveratrol, zinc PCA, kaolin, zeolite, aluminum starch octenylsuccinate, caprylic/capric triglyceride, polyglyceryl-2 triisostearate, silica dimethyl silylate, dimethicone crosspolymer, blue 1 lake, yellow 5 lake

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 eachPer 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
Eadem Sunsuede Daily Sunscreen And Blurring Primer Spf50 Plus 2.8 g/100g; 6.5 g/100g; 4.5 g/100g; 6.5 g/100gthis 87486-0100-01 EADEM, 1 bottle — — 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
Apr 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.

🔬 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 EADEM SUNSUEDE DAILY SUNSCREEN AND BLURRING PRIMER SPF50 PLUS (this brand).

Top reported reactions

Acute Myeloid Leukaemia2
Exposure To Toxic Agent2
Product Contamination Chemical2
Rash2
Anaphylactic Reaction1
Application Site Erythema1
Application Site Exfoliation1

Reporter sex

6 reports

Serious outcomes

Hospitalization2
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 2 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87486-0100-01 You're viewing this 1 BOTTLE, PLASTIC in 1 CARTON (87486-100-01) / 20 g in 1 BOTTLE, PLASTIC (87486-100-02) 2026-04-02 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 87486-100-01, 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: 87486-0100-01, written without dashes as 87486010001. 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 87486-0100-01, the first segment (87486) is the labeler code FDA assigned to EADEM, Inc.; the middle segment (0100) 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 EADEM, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
EADEM, 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 34 words ▾

Indications & Usage 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 50 words ▾

Dosage & Administration For Sunscreen Use: * Apply liberally and evenly 15 minutes before sun exposure, using multiple back and forth passes to ensure complete coverage to the area of application, especially to the areas above the lip, nose, and tops of ears. * Reapply at least every 2 hours

⚠️ Warnings 60 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 swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 15 words ▾

OTC - Active Ingredient Section Active ingredients Avobenzone (2.8%, Homosalate (6.5%) Octisalate (4.5%), Octocrylene (6.5%)

🧪 Inactive Ingredients 101 words ▾

Inactive ingredients Inactive ingredients diethylhexyl carbonate, dimethicone, synthetic wax, methyl methacrylate crosspolymer, butyloctyl salicylate, diphenylsiloxy phenyl trimethicone, C12-15 alkyl benzoate, isopropyl palmitate, diisostearyl malate, ethylhexyl isononanoate, isoeicosane, polyethylene, polymethylsilesquioxane, ethylene/propylene copolymer, dimethicone/vinyl dimethicone crosspolymer, camellia japonica seed oil, bis-behenyl/isostearyl/phytosteryl dimer dilinoleyl dimer dilinoleate, ananas sativus (pineapple) fruit extract, carica papaya (papaya) fruit extract, garcinia mangostana peel extract, mangifera indica (mango) fruit extract, morinda citrifolia extract, musa sapientum (banana) fruit extract, nephelium lappaceum branch/fruit/leaf extract, psidium guajava fruit extract, resveratrol, zinc PCA, kaolin, zeolite, aluminum starch octenylsuccinate, caprylic/capric triglyceride, polyglyceryl-2 triisostearate, silica dimethyl silylate, dimethicone crosspolymer, blue 1 lake, yellow 5 lake

🎯 Purpose 31 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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87482-0001-02 · Cellarkbio 87487-0100-02 · KSISTERS →
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.