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EWC Slow Lightweight Sunscreen SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE 30 mg/g; 100 mg/g; 50 mg/g Spray — NDC 81756-0001-00 package photo

EWC Slow Lightweight Sunscreen SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE 30 mg/g; 100 mg/g; 50 mg/g Spray

by EWC Ventures, LLC · 1 CAN in 1 CELLO PACK (81756-001-00) / 170 g in 1 CAN
NDC 81756-0001-00
🏷️ FDA NDC (as labeled) 81756-001-00 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) 81756-001-00
Product NDC 81756-001
11-digit billing NDC 81756000100
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W
UPC 0814783025040
Application # M020
SPL Set ID 063426b8-d1cf-4ee2-8ab8-ff007227eab8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-01
Route TOPICAL
Dosage form SPRAY
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Why two NDCs? The FDA registers this code as 81756-001-00 — 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 → 81756-0001-00. 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

LabelerEWC Ventures, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code81756
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?

EWC Slow Lightweight Sunscreen SPF 50 is a topical spray sunscreen formulated as an over-the-counter monograph product. It contains three UV-filtering active ingredients: avobenzone, homosalate, and octisalate. These ingredients are commonly used together in sunscreen products to absorb ultraviolet (UV) rays from the sun and help protect exposed skin from sun damage. The spray form is applied directly to the skin before outdoor activities.

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 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 WC51CA3418
    A fragrance compound derived from cinnamon, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII WAO5MNK9TU
    Benzyl salicylate is a fragrant chemical compound used as a flavor and scent ingredient in medicines. It helps mask unpleasant tastes or odors in liquid or oral formulations.
  • 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 8YOY78GNNX
    A fragrant essential oil derived from ylang-ylang tree flowers. It's used as a flavoring and fragrance agent to improve the taste or scent of medicines.
  • UNII P01OUT964K
    A fragrant plant-derived alcohol used as a flavoring agent and fragrance component in medicines. It provides taste and aroma to make the product more pleasant to use.
  • UNII 267F5Y81NT
    Coconut water is a natural liquid from inside coconut fruits. It's used in medicines as a vehicle or solvent to help dissolve and deliver active ingredients, and sometimes as a flavor or sweetening agent.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • 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 7X6O37OK2I
    A synthetic fragrance compound used as a flavoring agent or aromatic component in medicines. It adds pleasant taste or smell to make the medication more acceptable to patients.
  • UNII 8SQ0VA4YUR
    A fragrance compound derived from natural sources, used to add pleasant scent to the medicine. It serves as a flavoring or aromatic agent to mask unpleasant tastes or improve the product's sensory appeal.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII K17762966S
    A natural plant extract from the narcissus bulb used as a flavoring or fragrance ingredient in some medicines. It may help improve taste or smell of the product.
  • UNII T9296U138P
    A synthetic polymer derived from polyester chemistry, modified with a cyanodiphenylpropenoyl cap. It serves as a film-former and binder in pharmaceutical formulations, helping create protective coatings on tablets or improving product consistency.
  • UNII LZO6K1506A
    Rice bran oil is a natural oil extracted from rice grain. It's used in medicines as an emollient and solvent to help dissolve or suspend active ingredients and improve how the medicine feels when applied or taken.
  • 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.

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

The official label also statesalcohol denat., va/butyl maleate/isobornyl acrylate copolymer, amyl cinnamal, benzyl salicylate, butyloctyl salicylate, cananga odorata oil/extract, citronellol, cocos nucifera (coconut) water, geraniol, glycerin, hexyl cinnamal, hydroxycitronellal, leuconostoc/radish root ferment filtrate, narcissus tazetta bulb extract, oryza sativa (rice) bran oil, parfum (fragrance), polyester-8, water

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 mLPer 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
Avobenzone, Homosalate, Octisalate 30 mg/g; 100 mg/g; 50 mg/g 72036-0941-14 HARRIS 156 g — — FDA listed —
Sport Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 72476-0941-14 Retail 156 g — — FDA listed —
Sport Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 59450-0941-14 The 156 g — — FDA listed —
Broad Spectrum Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 72476-0948-14 Retail 156 g — — FDA listed —
Broad Spectrum Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 79481-0948-01 Meijer, 156 g — — FDA listed —
Broad Spectrum Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 75712-0948-14 Old 156 g — — FDA listed —
Avobenzone, Homosalate, Octisalate 30 mg/g; 100 mg/g; 50 mg/g 79481-0941-01 Meijer, 156 g — — FDA listed —
EWC Slow Lightweight Sunscreen SPF 50 30 mg/g; 100 mg/g; 50 mg/gthis 81756-0001-00 EWC 1 can — — FDA listed —
Avobenzone, Homosalate, Octisalate 30 mg/g; 100 mg/g; 50 mg/g 75712-0941-14 Old 156 g — — FDA listed —
Sport Sunscreen SPF 30 30 mg/g; 100 mg/g; 50 mg/g 63941-0149-14 Valu 156 g — — FDA listed —
Avobenzone, Homosalate, Octisalate 30 mg/g; 100 mg/g; 50 mg/g 76162-0941-14 Topco 156 g — — 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 AVOBENZONE, HOMOSALATE, OCTISALATE — the ingredient across all brands.

Top reported reactions

Skin Cancer65
Rash53
Pruritus37
Erythema29
Dyspnoea27
Malignant Melanoma27
Neoplasm Malignant27

Reporter sex

760 reports
Male · 35%
Female · 65%

Serious outcomes

Hospitalization109
Disabling26
Life-threatening12
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 232 7
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
81756-0001-00 You're viewing this 1 CAN in 1 CELLO PACK (81756-001-00) / 170 g in 1 CAN 2026-04-01 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 81756-001-00, 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: 81756-0001-00, written without dashes as 81756000100. 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 81756-0001-00, the first segment (81756) is the labeler code FDA assigned to EWC Ventures, LLC; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 EWC Ventures, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
EWC Ventures, 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.

📄 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 4 words ▾

Use helps prevent sunburn.

⏱️ Dosage and Administration 144 words ▾

Directions Shake well before using. Hold container 4 to 6 inches from the skin to apply. apply liberally and spread evenly by hand 15 minutes before sun exposure and as needed. reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours. Do not spray directly onto face.

Spray into hands and apply to face, avoiding the eye area. Do not apply in windy conditions. Use in a well-ventilated area.

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 of age: Ask a doctor.

⚠️ Warnings 78 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. do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120F. Stop use and ask doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Flammable: Do not use near heat, flame or while smoking.

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 3.00% Homosalate 10.00% Octisalate 5.00% Purpose Sunscreen

🧪 Inactive Ingredients 44 words ▾

Inactive ingredients alcohol denat., va/butyl maleate/isobornyl acrylate copolymer, amyl cinnamal, benzyl salicylate, butyloctyl salicylate, cananga odorata oil/extract, citronellol, cocos nucifera (coconut) water, geraniol, glycerin, hexyl cinnamal, hydroxycitronellal, leuconostoc/radish root ferment filtrate, narcissus tazetta bulb extract, oryza sativa (rice) bran oil, parfum (fragrance), polyester-8, water

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 81755-0004-92 · Shimmy 81759-0001-30 · BAMF →
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.