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Every. Single. Face. Watery SPF 50 Avobenzone, Homosalate, Octisalate, Octocrylene 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/100mL Lotion, 50 mL — NDC 75936-0652-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Every. Single. Face. Watery SPF 50 Avobenzone, Homosalate, Octisalate, Octocrylene 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/100mL Lotion, 50 mL — NDC 75936-652-03 (Billing 75936-0652-03)

by Supergoop, LLC · 50 mL in 1 BOTTLE

This is a package of 50 mL of Every. Single. Face. Watery SPF 50 Avobenzone, Homosalate, Octisalate, Octocrylene 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/100mL Lotion from Supergoop, LLC, marketed since Nov 2021 and currently FDA-listed.

NDC 75936-0652-03
🏷️ FDA NDC (as labeled) 75936-652-03 billing pads the product segment with a zero
This package
Contains50 mL Pack sizes3 compare ↓
Product page 75936-0652-01 Also comes in: 1.5 ml 75936-652-01 10 ml 75936-652-02
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 75936-652-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
75936 labeler · 652 product · 03 package
Package marketed since
Nov 11, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0816218029241
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 75936-652-03
Product NDC 75936-652
11-digit billing NDC 75936065203
UNII V06SV4M95S, G63QQF2NOX, 4X49Y0596W, 5A68WGF6WM
UPC 0816218029241
Application # M020
SPL Set ID d086a9b8-19e5-f713-e053-2995a90aa976
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-11-11
Route TOPICAL
Dosage form LOTION
Substance HOMOSALATE; AVOBENZONE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 75936-652-03 — 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 → 75936-0652-03. 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?

Every. Single. Face. Watery SPF 50 is a topical lotion sunscreen marketed as an over-the-counter monograph product. It contains four UV-filtering ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used to absorb and scatter ultraviolet radiation from the sun. This type of product is commonly applied to the skin to help reduce sun exposure.

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: 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
75936-0652-01 75936-652-01 Main listing 1.5 mL in 1 PACKET 2022-01-15 — Active
75936-0652-02 75936-652-02 10 mL in 1 TUBE 2022-01-15 — Active
75936-0652-03 You're viewing this 50 mL in 1 BOTTLE 2021-11-11 — Active

Pack size FAQ

What quantity is in this package?
This package contains 50 mL — 50 ml in 1 bottle.
How does this package differ from NDC 75936-0652-01?
Both are Every. Single. Face. Watery SPF 50 Avobenzone, Homosalate, Octisalate, Octocrylene 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/100mL Lotion — the drug itself is identical. This page's package is the 50 mL one, while NDC 75936-0652-01 is the 1.5 ml package.
What NDC number is used to bill for this package of Every. Single. Face. Watery SPF 50 Avobenzone, Homosalate, Octisalate, Octocrylene 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/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
Every. Single. Face. Watery SPF 50 9 g/100mL; 3 g/100mL; 5 g/100mL; 9 g/100mLthis 75936-0652-03 Supergoop, 50 ml — — 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

🏛️
2021
On the market since
Nov 2021
📍
2026
Currently FDA-listed
5 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 TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII JU3XHR8VWK
    A synthetic plastic polymer used as a film-coating agent. It forms a protective layer around tablets or capsules to control how and where the medicine dissolves in your digestive system.
  • UNII 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 3SCV180C9W
    Betaine is a naturally occurring organic compound found in plants and animals. In medicines, it acts as an osmoprotectant and stabilizer, helping maintain the product's moisture balance and preserve its chemical stability during storage.
  • UNII WL3883U2PO
    A natural resin derived from the caesalpinia spinosa plant, used as a binder and film-forming agent to help hold tablet ingredients together and create a protective coating on the medicine's surface.
  • 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 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 PWQ18YNR62
    A plant extract from garden cress sprouts used as a natural flavoring agent or botanical additive in medicines. It may contribute mild taste, aroma, or potential antioxidant properties to the formulation.
  • 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 B68LJT9544
    A fatty acid derivative used as a preservative and antimicrobial agent in topical medicines. It helps prevent bacterial and fungal growth to maintain product stability and safety.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII 92A6N0IQN9
    Hedychium coronarium root is a plant-derived ingredient, commonly known as butterfly ginger. It may be used as a fragrance, flavor enhancer, or natural coloring agent in formulations.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 8ZQ0AYU1TT
    Pullulan is a natural polysaccharide, a type of carbohydrate made from yeast. It acts as a binder and film-former to hold tablet ingredients together and create protective coatings on capsules.
  • UNII 2YGO1190AP
    A plant-derived carbohydrate from yeast or fungi, chemically modified to carry sodium and carboxyl groups. It acts as a thickener, stabilizer, and binder in medications to improve texture, consistency, and shelf life.
  • UNII 285CYO341L
    Sodium polyacrylate is a synthetic polymer that absorbs and holds water. In medicines, it acts as a disintegrant, helping tablets break apart quickly in the stomach, and as a binder, holding tablet ingredients together.
  • UNII GG8N28393G
    Tremella fuciformis, also called snow fungus, is a white jelly-like mushroom. In medications, it acts as a thickener and stabilizer to give the product a smooth texture and help keep ingredients evenly mixed.
  • 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.

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

The official label also statesInactive Ingredients: Water, Alcohol Denat., C12-15 Alkyl Benzoate, Propanediol, Dimethicone, Glycerin, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Maltodextrin, Hydroxyacetophenone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, 1,2 Hexanediol, Caprylyl Glycol, Pullulan, Sodium Polyacrylate, Betaine, Hedychium Coronarium Root Extract, Caesalpinia Spinosa Gum, Tremella Fuciformis Sporocarp Extract, Glyceryl Caprylate, Glyceryl Undecylenate, Sodium Carboxymethyl Beta-Glucan, Lepidium Sativum Sprout 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.

Manufacturer & labeler

LabelerSupergoop, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code75936
First marketedNov 2021
Product typeHuman Otc Drug
Portfolio61 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 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Stop use and ask a doctor if rash occurs.

⏱️ Dosage and Administration 99 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 early skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF calue of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m.-2p.m. Wear long-sleeved shirts, pants, hats, and sunglasses Reapply at least every 2 hours Children under 6 months: Ask a doctor

⚠️ Warnings 26 words ▾

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

🧪 Active Ingredient 12 words ▾

Active Ingredients Purpose Avobenzone 3% Sunscreen Homosalate 9% Octisalate 5% Octocrylene 9%

🧪 Inactive Ingredients 49 words ▾

Inactive Ingredients: Water, Alcohol Denat., C12-15 Alkyl Benzoate, Propanediol, Dimethicone, Glycerin, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Maltodextrin, Hydroxyacetophenone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, 1,2 Hexanediol, Caprylyl Glycol, Pullulan, Sodium Polyacrylate, Betaine, Hedychium Coronarium Root Extract, Caesalpinia Spinosa Gum, Tremella Fuciformis Sporocarp Extract, Glyceryl Caprylate, Glyceryl Undecylenate, Sodium Carboxymethyl Beta-Glucan, Lepidium Sativum Sprout Extract.

🎯 Purpose 30 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

📄 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.

📄 Other Information 12 words ▾

Protect the product in this container from excessive heat and direct sun.

📄 Package Label / Principal Display Panel 29 words ▾

Supergoop! EVERY. SINGLE. FACE. WATERY LOTION SPF 50 Broad Spectrum Sunscreen SPF 50 PA++++ Water & Sweat Resistant (40 minutes) 1.7 fl. oz./ 50 ml. Carton 50 ml bottle

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

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 2 other package presentations of this same product, including 1.5 ml (75936-0652-01), 10 ml (75936-0652-02). 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.
← 75936-0651-01 · Supergoop 75936-0653-01 · 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.