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Unseen Sunscreen SPF 50 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE 5 mg/100mL; 9 mg/100mL; 3 mg/100mL; 7 mg/100mL Lotion — NDC 75936-0641-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Unseen Sunscreen SPF 50 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE 5 mg/100mL; 9 mg/100mL; 3 mg/100mL; 7 mg/100mL Lotion — NDC 75936-641-02 (Billing 75936-0641-02)

by Supergoop LLC · 1 TUBE in 1 BOX / 74 mL in 1 TUBE

This is a package of Unseen Sunscreen SPF 50 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE 5 mg/100mL; 9 mg/100mL; 3 mg/100mL; 7 mg/100mL Lotion from Supergoop LLC, marketed since Sep 2024 and currently FDA-listed. It is the main listing for this product, which comes in 5 package sizes.

NDC 75936-0641-02
🏷️ FDA NDC (as labeled) 75936-641-02 billing pads the product segment with a zero
This package
Contains74 mL in 1 tube Pack sizes5 compare ↓
Main listing for product 75936-641 · Also comes in: 50 mL 75936-641-04 20 mL 75936-641-06 1.5 ml 75936-641-08 10 ml 75936-641-07
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 75936-641-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
75936 labeler · 641 product · 02 package
Package marketed since
Sep 9, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7593664102 4
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 75936-641-02
Product NDC 75936-641
11-digit billing NDC 75936064102
UNII 4X49Y0596W, 5A68WGF6WM, G63QQF2NOX, V06SV4M95S
Application # M020
SPL Set ID 21b3491f-7b02-9bc5-e063-6294a90a0dc3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-09
Route TOPICAL
Dosage form LOTION
Substance OCTISALATE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
Why two NDCs? The FDA registers this code as 75936-641-02 — 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 → 75936-0641-02. 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.

Clinical

🧪 What is this product?

Unseen Sunscreen SPF 50 is a topical lotion marketed as an over-the-counter sunscreen under FDA's OTC monograph rules. It contains four UV-filtering ingredients (octocrylene, homosalate, octisalate, and avobenzone) that are typically used together to absorb and scatter ultraviolet light from the sun. These chemical sunscreen agents function to help reduce sun exposure to the skin when applied topically. The product is formulated as a lotion for direct application to exposed skin surfaces.

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 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.
Try another pack size: 50 mL 20 mL 1.5 ml 10 ml
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
75936-0641-02 You're viewing this Main listing 1 TUBE in 1 BOX / 74 mL in 1 TUBE 2024-09-09 — Active
75936-0641-04 75936-641-04 1 TUBE in 1 BOX / 50 mL in 1 TUBE 2024-09-09 — Active
75936-0641-06 75936-641-06 1 TUBE in 1 BOX / 20 mL in 1 TUBE 2024-09-09 — Active
75936-0641-07 75936-641-07 10 mL in 1 TUBE Sample 2024-09-09 — Active
75936-0641-08 75936-641-08 1.5 mL in 1 PACKET Sample 2024-09-09 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 box / 74 ml in 1 tube.
What NDC number is used to bill for this package of Unseen Sunscreen SPF 50 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE 5 mg/100mL; 9 mg/100mL; 3 mg/100mL; 7 mg/100mL Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Unseen Sunscreen SPF 50 5 mg/100mL; 9 mg/100mL; 3 mg/100mL; 7 mg/100mLthis 75936-0641-02 Supergoop 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

🏛️
2024
On the market since
Sep 2024
📍
2026
Currently FDA-listed
2 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.

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 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 3V5U97P248
    A synthetic organic compound used as a UV filter and stabilizer in medications. It helps protect the drug from light degradation and may improve shelf life in formulations exposed to sunlight.
  • UNII RO266O364U
    Dimethicone is a silicone-based lubricant and anti-foaming agent. It reduces friction between particles and prevents foam formation in liquid or semi-solid medicines, helping with smooth mixing and texture.
  • 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 O4I3UFO6ZF
    A silicone-based polymer blend that acts as an emulsifier and texture modifier. It helps keep oil and water mixed together in the formulation and gives the product a smooth, spreadable consistency.
  • 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 CA2Y0FE3FX
    A salt derived from licorice root extract, used as a flavoring agent and sweetener. It may also help soothe and protect mucous membranes in throat lozenges and cough products.
  • UNII 21RND18XRR
    A seaweed extract used as a thickener and stabilizer in medicines. It helps maintain consistent texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • UNII Q47ST02F58
    A waxy, solid oil derived from jojoba plant seeds. It acts as a binder and emollient to help hold ingredients together and improve texture in topical or oral formulations.
  • 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 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 3HH93SL2H9
    A plant-derived oil made from meadowfoam seeds. It acts as an emollient and lubricant in medicines, helping soften formulations and improve how ingredients mix together.
  • 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 W4TKW9D5GG
    Physalis angulata is a plant extract used as a natural flavoring or coloring agent in some medicines. It may also serve as a botanical ingredient to support the product's formulation.
  • UNII 59Z907ZB69
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles, helping powders and tablets flow smoothly during manufacturing and use.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and 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.

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

The official label also statesIsododecane, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Dimethicone Crosspolymer, Caprylic/Capric Triglyceride, Butyrospermum Parkii (Shea) Butter, Physalis Angulata Extract, Himanthalia Elongata Extract, Meadowfoam Estolide, Tocopherol, Jojoba Esters, Polymethylsilsesquioxane, Caprylyl Glycol, Diethylhexyl Syringylidenemalonate, Silica, Bisabolol, Dipotassium Glycyrrhizate.

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

LabelerSupergoop LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code75936
First marketedSep 2024
Product typeHuman Otc Drug
Portfolio18 products on file

More NDCs from Supergoop LLC labeler code 75936

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Stop use and ask a doctor if rash occurs

⏱️ Dosage and Administration 94 words ▾

Directions Apply generously and evenly 15 minutes before sun exposure Reapply after 40 minutes of swimming or sweating Immediately after towel drying at least every 2 hours 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 a Broad Spectrum SPF value 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-sleeved shirts, pants, hats, and sunglasses Children under 6 months: Ask a doctor

⚠️ Warnings 25 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

🧪 Active Ingredient 8 words ▾

Avobenzone 3%, Homosalate 7%, Octisalate 5%, Octocrylene 9%

🧪 Inactive Ingredients 36 words ▾

Isododecane, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Dimethicone Crosspolymer, Caprylic/Capric Triglyceride, Butyrospermum Parkii (Shea) Butter, Physalis Angulata Extract, Himanthalia Elongata Extract, Meadowfoam Estolide, Tocopherol, Jojoba Esters, Polymethylsilsesquioxane, Caprylyl Glycol, Diethylhexyl Syringylidenemalonate, Silica, Bisabolol, Dipotassium Glycyrrhizate.

🎯 Purpose 28 words ▾

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

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. If product is swallowed, get medical help, or contact a poison control center right away.

📄 Package Label / Principal Display Panel 24 words ▾

Unseen Sunscreen SPF 50 Broad Spectrum Sunscreen SPF 50 PA+++ Water & Sweat Resistance (40 minutes) 1.7 fl oz / 50 mL Carton Tube

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

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 OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE — the ingredient across all brands.

Top reported reactions

Fatigue15
Dyspnoea14
Dizziness12
Headache12
Anxiety11
Chronic Kidney Disease11
Pain11

Age at onset

Child2
Adult14
Elderly21

Reporter sex

230 reports
Male · 33%
Female · 67%

Serious outcomes

Hospitalization46
Disabling9
Life-threatening7
Death6
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 12 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.

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: this package is listed as actively marketed, with no marketing end date reported by Supergoop LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 4 other package presentations of this same product, including 1 tube (75936-0641-04), 1 tube (75936-0641-06), 1.5 ml (75936-0641-08). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Supergoop LLC 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.
← 75936-0640-02 · Supergoop 75936-0644-02 · Supergoop! →
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.