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AGE20S SUNSCREEN DUO Zinc Oxide, Avobenzone, Homosalate, Octisalate, Octocrylene Kit — NDC 67225-5333-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

AGE20S SUNSCREEN DUO Zinc Oxide, Avobenzone, Homosalate, Octisalate, Octocrylene Kit — NDC 67225-5333-1 (Billing 67225-5333-01)

by Aekyung Industrial Co., Ltd. · 1 KIT in 1 CARTON * 1 TUBE in 1 BOX / 50 g in 1 TUBE * 1 TUBE in 1 BOX / 50 g in 1 TUBE

This is a package of AGE20S SUNSCREEN DUO Zinc Oxide, Avobenzone, Homosalate, Octisalate, Octocrylene Kit from Aekyung Industrial Co., Ltd., marketed since Apr 2026 and currently FDA-listed. It is this product's only package size.

NDC 67225-5333-01
🏷️ FDA NDC (as labeled) 67225-5333-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 67225-5333-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
67225 labeler · 5333 product · 1 package
Package marketed since
Apr 8, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 6722553331 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 67225-5333-1
Product NDC 67225-5333
11-digit billing NDC 67225533301
Application # M020
SPL Set ID 4eef11cd-85a1-0e44-e063-6394a90a5d44
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-08
Route TOPICAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 67225-5333-1 — a 5-4-1 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 package segment → 67225-5333-01. 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.

Clinical

🧪 What is this product?

This is a topical sunscreen kit containing five active ingredients commonly used to protect skin from ultraviolet (UV) light. Zinc oxide and avobenzone function as broad-spectrum UV filters that absorb and reflect UV rays. Homosalate, octisalate, and octocrylene are additional UV-filtering agents that work together with the other ingredients to provide sun protection. This product is marketed as an over-the-counter monograph drug, meaning it follows the FDA's established rules for sunscreen products rather than being individually reviewed.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
67225-5333-01 You're viewing this Main listing 1 KIT in 1 CARTON * 1 TUBE in 1 BOX / 50 g in 1 TUBE * 1 TUBE in 1 BOX / 50 g in 1 TUBE 2026-04-08 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Age20S Sunscreen Duothis 67225-5333-01 Aekyung 1 kit — — 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.

What it looks like

Color white
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.

From the label’s inactive-ingredient sectionAGE20S UV DEFENSE HYDRO CALMING SUNSCREEN Water, Propanediol, Butyloctyl Salicylate, Polyglyceryl-3 Distearate, Silica, Microcrystalline Cellulose, C13-15 Alkane, Panthenol, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extr Hydroxyhydrocinnamate, Benzotriazolyl Dodecyl p-Cresol, Hydroxyacetophenone, Sodium Stearoyl Glutamate, Butylene Glycol, Allantoin, Ammonium Polyacryloyldimethyl Taurate, Cetear Oleic Acid, Caprylhydroxamic Acid, Ethanol, Cellulose Gum, 1,2-Hexanediol, Oryza Sativa (Rice) Bran Extract, Scutellaria Baicalenesis Root Extract, Tris(Tetramethylhy- droxypiperidinol) Hyaluronic Acid, Ceramide NP AGE20S UV MINERAL PRIMING SUNSCREEN Water, Dimethicone,Butyloctyl Salicylate, Propanediol, Ethylhexyl Methoxycrylene, PEG-10 Dimethicone, Phenyl Trimethicone, Silica, Zeolite, Caprylyl Methicone, Glyceryl Glucoside, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, Glycerin, Magnesium Sulfate, Dimethicone/Vinyl Dimethicone Crosspolymer, Panthenol, Calcium Aluminum Borosilicate, Aloe Barbadensis Leaf Extract, Dipropylene Glycol, Benzotriazolyl Dodecyl p-Cresol, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Triethoxycaprylylsilane, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Hydroxyacetophenone Allantoin, Caprylyl Glycol, Caprylhydroxamic Acid, Titanium Dioxide, Butylene Glycol, Tin Oxide, 1,2-Hexanediol, Dibutyl Adipate Neopentyl Glycol Diheptanoate, C15-23 Alkane, Hydrogenated Lecithin, Cetearyl Alcohol, Stearic Acid, C13-14 Alkane, Bakuchiol Camellia Sinensis Leaf Extract, Hyaluronic Acid, Pentasodium Tetracarboxymethyl Heptadecanoyl Dipeptide-12, Tocopherol, Ceramide NP, Ceramide NS, Cholesterol, Phytosphingosine, Ceramide AP, Ceramide AS, Ceramide EOP

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerAekyung Industrial Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code67225
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio64 products on file

More NDCs from Aekyung Industrial Co., Ltd. labeler code 67225

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

■ Helps prevent sunburn. ■ If used as directed with other sun protection measures (see Driections), decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 97 words ▾

■ apply liberally 15 minutes before sun exposure. ■ children under 6 months of age: Ask a doctor. ■ 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 ■ reapply at least every 2 hours. ■ use a water resistant sunscreen if swimming or sweating

⚠️ Warnings 4 words ▾

For external use only

🧪 Active Ingredient 22 words ▾

AGE20S UV DEFENSE HYDRO CALMING SUNSCREEN Avobenzone 2.70% Homosalate 7.00% Octisalate 4.50% Octocrylene 9.00% AGE20S UV MINERAL PRIMING SUNSCREEN Zinc Oxide 14.68%

🧪 Inactive Ingredients 172 words ▾

AGE20S UV DEFENSE HYDRO CALMING SUNSCREEN Water, Propanediol, Butyloctyl Salicylate, Polyglyceryl-3 Distearate, Silica, Microcrystalline Cellulose, C13-15 Alkane, Panthenol, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extr Hydroxyhydrocinnamate, Benzotriazolyl Dodecyl p-Cresol, Hydroxyacetophenone, Sodium Stearoyl Glutamate, Butylene Glycol, Allantoin, Ammonium Polyacryloyldimethyl Taurate, Cetear Oleic Acid, Caprylhydroxamic Acid, Ethanol, Cellulose Gum, 1,2-Hexanediol, Oryza Sativa (Rice) Bran Extract, Scutellaria Baicalenesis Root Extract, Tris(Tetramethylhy- droxypiperidinol) Hyaluronic Acid, Ceramide NP AGE20S UV MINERAL PRIMING SUNSCREEN Water, Dimethicone ,Butyloctyl Salicylate, Propanediol, Ethylhexyl Methoxycrylene, PEG-10 Dimethicone, Phenyl Trimethicone, Silica, Zeolite, Caprylyl Methicone, Glyceryl Glucoside, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, Glycerin, Magnesium Sulfate, Dimethicone/Vinyl Dimethicone Crosspolymer, Panthenol, Calcium Aluminum Borosilicate, Aloe Barbadensis Leaf Extract, Dipropylene Glycol, Benzotriazolyl Dodecyl p-Cresol, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Triethoxycaprylylsilane, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Hydroxyacetophenone Allantoin, Caprylyl Glycol, Caprylhydroxamic Acid, Titanium Dioxide, Butylene Glycol, Tin Oxide, 1,2-Hexanediol, Dibutyl Adipate Neopentyl Glycol Diheptanoate, C15-23 Alkane, Hydrogenated Lecithin, Cetearyl Alcohol, Stearic Acid, C13-14 Alkane, Bakuchiol Camellia Sinensis Leaf Extract, Hyaluronic Acid, Pentasodium Tetracarboxymethyl Heptadecanoyl Dipeptide-12, Tocopherol, Ceramide NP, Ceramide NS, Cholesterol, Phytosphingosine, Ceramide AP, Ceramide AS, Ceramide EOP

🎯 Purpose 1 words ▾

Sunscree

📄 Do Not Use 6 words ▾

■ on damaged or broken skin.

📄 When Using This Product 10 words ▾

■ keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 10 words ▾

Stop use and ask a doctor if ■ rash occurs.

📄 Keep Out of Reach of Children 12 words ▾

If swallowed, get medical help or contact poison control center right away.

📄 Other Information 17 words ▾

■ Protect the product in the container from excessive heat and avoid storing it under direct sun.

📄 Package Label / Principal Display Panel 3 words ▾

Sunscreen_PR_Outbox_1 Sunscreen_PR_Outbox_2 Sunscreen_PR

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 Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 Aekyung Industrial Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Aekyung Industrial 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.
← 67225-5331-02 · Aekyung 67226-1021-01 · Vivier →
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.