Home › NDC Lookup › Ingredients › Titanium Dioxide, Octinoxate, Octisalate › 71261-0027-02
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE 65.1 mg/g; 67 mg/g; 40 mg/g Cream — NDC 71261-0027-02 package photo

JUNGSAEMMOOL Essential Skin Nuder Cushion Fair TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE 65.1 mg/g; 67 mg/g; 40 mg/g Cream

by Jungsaemmool Beauty Co., Ltd. · 2 CONTAINER in 1 CARTON (71261-027-02) / 14 g in 1 CONTAINER (71261-027-01)
NDC 71261-0027-02
🏷️ FDA NDC (as labeled) 71261-027-02 billing pads the product segment with a zero
This package
Contains14 g in 1 container Pack sizes3 compare ↓
Also comes in: 14 g 71261-0027-05 14 g 71261-0027-03
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 71261-027-02
Product NDC 71261-027
11-digit billing NDC 71261002702
UNII 15FIX9V2JP, 4Y5P7MUD51, 4X49Y0596W
Application # M020
SPL Set ID 3a43c7c0-7468-4b7a-95b9-f03e37f1b49b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-29
Route TOPICAL
Dosage form CREAM
Substance TITANIUM DIOXIDE; OCTINOXATE; OCTISALATE
Why two NDCs? The FDA registers this code as 71261-027-02 — 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 → 71261-0027-02. 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.

🏭 Manufacturer & labeler

LabelerJungsaemmool Beauty Co., Ltd.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code71261
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio15 products on file
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 an over-the-counter topical cream cosmetic product marketed as a cushion foundation. It contains three active ingredients that function as ultraviolet light filters: octinoxate and octisalate, which absorb UV rays, and titanium dioxide, which reflects them. Products of this type are typically used to provide sun protection and cosmetic coverage to the face.

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 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 S7ZA3CCJ4M
    A synthetic polymer made from acrylic compounds and silicone, this substance forms a flexible protective coating on tablet or capsule surfaces. It helps control medicine release into your body and protects the active ingredient from moisture and air.
  • UNII 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII Q95M2P1KJL
    A silicone-based ingredient that acts as a lubricant and glidant. It helps the tablet or capsule move smoothly through manufacturing equipment and improves powder flow during production.
  • UNII 134647WMX4
    Cetyl ethylhexanoate is a synthetic oil used as an emollient and texture enhancer in medications. It helps soften the skin, improve spreadability, and provides a smooth feel to topical formulations.
  • UNII 8INO2K35FA
    A silicone-based compound that mixes oil and water components together. It acts as an emulsifier and helps distribute ingredients evenly throughout the formulation, improving texture and stability.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • 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 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 X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • 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 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 JY81OXM1OM
    A plant-based oil from coconut that has been chemically treated to solidify it. It acts as a binder and filler to help hold tablet ingredients together and give the pill its shape and firmness.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII 287GF3Y3WC
    PEG-10 Dimethicone is a silicone-based compound that acts as an emulsifier and surfactant in medicines. It helps blend water and oil-based ingredients together and reduces surface tension to improve how the product spreads and feels.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • 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 KM7N50LOS6
    Tin oxide is an inorganic mineral compound used in medicines as a colorant and opacifying agent. It provides white or off-white color to tablets, capsules, and coatings while helping make formulations less transparent.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 5041RX63GN
    A synthetic silicon-based polymer used as a glidant and anti-caking agent. It helps powder particles flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 9G1ZW13R0G
    A silicone-based polymer that reduces surface tension and improves how liquid medicines spread and are absorbed. It acts as a wetting agent and surfactant in topical formulations.
  • UNII YA22H34H9Q
    A chelating agent derived from sodium and organic compounds. It binds to metal ions in the formulation to improve stability and prevent unwanted chemical reactions that could degrade the medicine.
  • UNII KFR5QEN0N9
    A synthetic plastic polymer that helps form a protective film coating on the medicine. It's used as a binder and film-former to hold the tablet or capsule together and control how quickly the drug dissolves.
  • 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.

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

The official label also statesWater, Cyclopentasiloxane, Titanium Dioxide (CI 77891), Glycerin, Propanediol, Trimethylsiloxysilicate, PEG-10 Dimethicone, Cetyl Ethylhexanoate, Trisiloxane, Synthetic Fluorphlogopite, 1,2-Hexanediol, Caprylyl Methicone, Dimethicone, Hydrogenated Coconut Oil, Polypropylsilsesquioxane, VP/Hexadecene Copolymer, Iron Oxides (CI 77492), Disteardimonium Hectorite, Magnesium Sulfate, Acrylates/Dimethicone Copolymer, Cetyl PEG/PPG-10/1 Dimethicone, Stearic Acid, Alumina, Aluminum Hydroxide, Glyceryl Caprylate, Triethoxycaprylylsilane, Iron Oxides (CI 77491), Fragrance(Parfum), Dimethicone Crosspolymer, Iron Oxides (CI 77499), Trisodium Ethylenediamine Disuccinate, BHT, Mica (CI 77019), Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Tin Oxide (CI 77861)

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 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: 14 g 14 g
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
JUNGSAEMMOOL Essential Skin Nuder Cushion N-Light 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0032-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Medium 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0033-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair 65.1 mg/g; 67 mg/g; 40 mg/gthis 71261-0027-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair Pink 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0029-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Light 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0030-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Bronze 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0039-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair Light 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0028-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Pink Light 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0031-02 Jungsaemmool 14 g — — FDA listed —
JUNGSAEMMOOL Essential Skin Nuder Cushion Medium Deep 65.1 mg/g; 67 mg/g; 40 mg/g 71261-0034-02 Jungsaemmool 14 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

🏛️
2024
On the market since
Jul 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
71261-0027-02 You're viewing this 2 CONTAINER in 1 CARTON (71261-027-02) / 14 g in 1 CONTAINER (71261-027-01) 2024-07-29 Active
71261-0027-03 1 CONTAINER in 1 CARTON (71261-027-03) / 14 g in 1 CONTAINER (71261-027-01) 2026-04-17 Active
71261-0027-05 1 POUCH in 1 CARTON (71261-027-05) / 14 g in 1 POUCH (71261-027-04) 2026-04-17 Active

Pack size FAQ

What quantity is in NDC 71261-0027-02?
NDC 71261-0027-02 is listed by the FDA — 2 container in 1 carton / 14 g in 1 container.
What NDC number is used to bill for this package of JUNGSAEMMOOL Essential Skin Nuder Cushion Fair TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE 65.1 mg/g; 67 mg/g; 40 mg/g Cream?
Bill NDC 71261-0027-02 — the 11-digit billing format is 71261002702. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 71261-027-02, 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: 71261-0027-02, written without dashes as 71261002702. 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 71261-0027-02, the first segment (71261) is the labeler code FDA assigned to Jungsaemmool Beauty Co., Ltd.; the middle segment (0027) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Jungsaemmool Beauty Co., Ltd.. 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 pouch (71261-0027-05), 14 g (71261-0027-03). 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?
Jungsaemmool Beauty 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.

📄 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 28 words ▾

Helps prevent sunburn If used as directed with other sun protection measures (see Directions) decrease the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 96 words ▾

For sunscreen use: Apply liberally 15 minutes before sun exposure Reapply at least every two hours Use a water-resistant sunscreen if swimming or sweating 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 of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm.

2) Wear long-sleeve shirts, pants, hats, and sunglasses Ask a doctor to use for children under 6 months

⚠️ Warnings 34 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. Stop using and ask a doctor if rash occurs.

🧪 Active Ingredient 7 words ▾

Titanium Dioxide 6.51% Octinoxate 6.70% Octisalate 4.00%

🧪 Inactive Ingredients 72 words ▾

Water, Cyclopentasiloxane, Titanium Dioxide (CI 77891), Glycerin, Propanediol, Trimethylsiloxysilicate, PEG-10 Dimethicone, Cetyl Ethylhexanoate, Trisiloxane, Synthetic Fluorphlogopite, 1,2-Hexanediol, Caprylyl Methicone, Dimethicone, Hydrogenated Coconut Oil, Polypropylsilsesquioxane, VP/Hexadecene Copolymer, Iron Oxides (CI 77492), Disteardimonium Hectorite, Magnesium Sulfate, Acrylates/Dimethicone Copolymer, Cetyl PEG/PPG-10/1 Dimethicone, Stearic Acid, Alumina, Aluminum Hydroxide, Glyceryl Caprylate, Triethoxycaprylylsilane, Iron Oxides (CI 77491), Fragrance(Parfum), Dimethicone Crosspolymer, Iron Oxides (CI 77499), Trisodium Ethylenediamine Disuccinate, BHT, Mica (CI 77019), Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Tin Oxide (CI 77861)

🎯 Purpose 1 words ▾

Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 71258-0022-01 · Progenics 71261-0028-02 · Jungsaemmool →
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.