Home › NDC Lookup › Ingredients › Titanium Dioxide Zinc Oxide › 82141-2328-01
toty Ilumina CC Cream 1W Titanium Dioxide, Zinc Oxide 9 g/100g; 6.3 g/100g Cream — NDC 82141-2328-01 package photo

toty Ilumina CC Cream 1W Titanium Dioxide, Zinc Oxide 9 g/100g; 6.3 g/100g Cream

by Chipican LLC · 1 TUBE in 1 CARTON (82141-2328-1) / 40 g in 1 TUBE
NDC 82141-2328-01
🏷️ FDA NDC (as labeled) 82141-2328-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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

⚠️
Other active recalls for Titanium Dioxide, Zinc Oxide (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Sep 3, 2024 — Microbial Contamination of Non-Sterile Product (Vivier Pharma, Inc.) · FDA recall D-0662-2024
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 82141-2328-1
Product NDC 82141-2328
11-digit billing NDC 82141232801
UNII SOI2LOH54Z, 15FIX9V2JP
Application # M020
SPL Set ID e4efe14e-7d46-78c0-e053-2995a90a2364
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-10-01
Route TOPICAL
Dosage form CREAM
Substance TITANIUM DIOXIDE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 82141-2328-1 — 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 → 82141-2328-01. 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.

🏭 Manufacturer & labeler

LabelerChipican LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code82141
First marketedOct 2022
Product typeHuman Otc Drug
Portfolio32 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?

Toty Ilumina CC Cream is a topical cream containing titanium dioxide and zinc oxide as active ingredients. Both minerals are commonly used in over-the-counter skincare products to provide coverage and help protect skin. This product is marketed as an OTC monograph drug, meaning it is made under FDA's established rules for this category of cosmetic-pharmaceutical products rather than as an individually approved application. The cream form allows for easy application to facial skin.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII B2JUC5N9EH
    A synthetic compound derived from coconut oil and butylene glycol, used as an emollient and emulsifier to help blend oil and water components together in formulations.
  • 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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII V5RS026Q0H
    A synthetic polymer made by combining several plastic-like compounds. It forms a protective coating on tablets or capsules to control where and when the medicine dissolves in the digestive system.
  • 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 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 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 8FA93U5T67
    A waxy substance made from plant oils that acts as an emulsifier and thickener. It helps mix oil and water components in the medicine and gives the product a smooth texture.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII ICS790225B
    A plant-derived cleaning agent made from coconut oil and glucose. It works as a surfactant and emulsifier to help mix oil and water-based ingredients together in the formulation.
  • UNII 609A3V1SUA
    A silky liquid derived from caprylic acid that acts as an emollient and solvent in formulations. It helps dissolve active ingredients and improves the spreadability and feel of lotions, creams, and topical products.
  • UNII 6OA5ZDY41O
    A synthetic oily liquid made by combining propylene glycol with benzoic acid. It works as a plasticizer and solvent in medicines, helping to soften coatings, improve texture, and keep ingredients blended together in liquid or semi-solid formulations.
  • UNII QI9A6U005W
    A synthetic cleansing agent derived from coconut oil and polyethylene glycol. In medicines, it acts as a surfactant to help mix oil and water-based ingredients and improve how the product spreads or dissolves.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • 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 V42034O9PU
    A fatty alcohol derived from coconut or palm oil. It serves as an emulsifier and thickener to help blend oil and water in creams or lotions, and improves the product's texture and consistency.
  • UNII 6AK28695LF
    A plant-derived surfactant made from myristic acid and glucose. It helps dissolve or suspend other ingredients and improves how the medicine spreads or absorbs in the body.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 0F897O3O4M
    A naturally occurring alcohol derived from plants or synthesized chemically. It functions as a preservative and flavoring agent in medicines, helping prevent microbial growth and add pleasant taste to oral products.
  • UNII BG58BW230G
    A plant extract from golden polypody fern leaves. Used in formulations for its traditional skin-soothing properties and as a natural botanical ingredient to support the product's intended effects on skin health and appearance.
  • UNII 80D2J6361M
    A synthetic oily compound made from propylene glycol, stearyl alcohol, and benzoic acid. It acts as an emulsifier and solvent in formulations, helping mix oil and water-based ingredients and improve product texture.
  • 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 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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 OLX698AH5P
    A clay mineral processed with a quaternary ammonium compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • 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.

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

The official label also statesNDCs 82141-2327-1, 82141-2328-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala (Polypodium leucotomos) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Tea (Camellia sinensis) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients. NDCs 82141-2329-1, 82141-2330-1, 82141-2331-1, 82141-2332-1, 82141-2333-1 82141-2334-1, 82141-2336-1 & 82141-2338-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala (Polypodium leucotomos) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea (Camellia sinensis) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients. NDCs 82141-2335-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala (Polypodium leucotomos) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea (Camellia sinensis) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Triethoxycaprylylsilane, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients. NDCs 82141-2337-1 & 82141-2339-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Ceteareth-25, Glyceril Stearate, PEG-100 Stearate, Propylene Glycol, Dipropylene Glycol Dibenzoate, Silica, Phenoxyethanol, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Panthenol, Calaguala (Polypodium leucotomos) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea (Camellia sinensis) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Tocopheryl Acetate, Steareth-21, Steareth-2, Triethoxycaprylylsilane, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499). * Contains one or more of these ingredients. NDCs 82141-2340-1 & 82141-2341-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Silica, Phenoxyethanol, Phenylpropanol, Disodium Ethylene Dicocamide PEG-15 Disulfate, Panthenol, Calaguala (Polypodium leucotomos) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea (Camellia sinensis) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Tocopheryl Acetate, Glyceryl Stearate, PEG-100 Stearate, Steareth-21, Steareth-2, Triethoxycaprylylsilane, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499). * Contains one or more of these ingredients.

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.
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
toty Ilumina CC Cream 1N 9 g/100g; 6.3 g/100g 82141-2327-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 5W 9 g/100g; 6.3 g/100g 82141-2339-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 2N 9 g/100g; 6.3 g/100g 82141-2330-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 1C 9 g/100g; 6.3 g/100g 82141-2329-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 4C 9 g/100g; 6.3 g/100g 82141-2338-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 4N 9 g/100g; 6.3 g/100g 82141-2336-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 4W 9 g/100g; 6.3 g/100g 82141-2337-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 5W1 9 g/100g; 6.3 g/100g 82141-2340-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 3C 9 g/100g; 6.3 g/100g 82141-2335-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 5W2 9 g/100g; 6.3 g/100g 82141-2341-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 1W 9 g/100g; 6.3 g/100gthis 82141-2328-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 3N 9 g/100g; 6.3 g/100g 82141-2333-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 2W 9 g/100g; 6.3 g/100g 82141-2331-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 2C 9 g/100g; 6.3 g/100g 82141-2332-01 Chipican 1 tube — — FDA listed —
toty Ilumina CC Cream 3W 9 g/100g; 6.3 g/100g 82141-2334-01 Chipican 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

🏛️
2022
On the market since
Oct 2022
📍
2026
Currently FDA-listed
4 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.

🔬 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 toty Ilumina CC Cream 1W (this brand).

Top reported reactions

Application Site Acne1
Application Site Hypersensitivity1
Application Site Vesicles1

Reporter sex

1 reports
Reports over time (by year) — tap or hover for the count & year
2025 2026 1 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
82141-2328-01 You're viewing this 1 TUBE in 1 CARTON (82141-2328-1) / 40 g in 1 TUBE 2022-10-01 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 82141-2328-1, 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: 82141-2328-01, written without dashes as 82141232801. 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 82141-2328-01, the first segment (82141) is the labeler code FDA assigned to Chipican LLC; the middle segment (2328) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Chipican LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Chipican 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 29 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.

⏱️ Dosage and Administration 92 words ▾

Apply liberally 15 minutes behore sun exposure Reapply at least every 2 hours Use a water-resistant sunscreen if swimmimg 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 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 35 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. Stop use and ask a doctor if Rash occurs

📦 Storage and Handling 26 words ▾

Other Information Shake well before use Do not expose the product to high temperatures Protect the product in this container from excessive heat and direct sun

🧪 Active Ingredient 8 words ▾

Active Ingredients Titanium Dioxide 9% Zinc Oxide 6.3%

🧪 Inactive Ingredients ~2 min read ▾

Inactive Ingredients NDCs 82141-2327-1, 82141-2328-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala ( Polypodium leucotomos ) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Tea ( Camellia sinensis ) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients.

NDCs 82141-2329-1, 82141-2330-1, 82141-2331-1, 82141-2332-1, 82141-2333-1 82141-2334-1, 82141-2336-1 & 82141-2338-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala ( Polypodium leucotomos ) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea ( Camellia sinensis ) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients.

NDCs 82141-2335-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Dicaprylyl Carbonate, Coco Glucoside, Myristyl Alcohol, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Silica, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Myristyl Glucoside, Panthenol, Calaguala ( Polypodium leucotomos ) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea ( Camellia sinensis ) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Stearalkonium Hectorite, Propylene Carbonate, Tocopheryl Acetate, BHT, Citric Acid, Disodium EDTA, Triethoxycaprylylsilane, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499), Titanium Dioxide* (CI 77891), Bismuth Oxychloride* (CI 77163). * Contains one or more of these ingredients.

NDCs 82141-2337-1 & 82141-2339-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Ceteareth-25, Glyceril Stearate, PEG-100 Stearate, Propylene Glycol, Dipropylene Glycol Dibenzoate, Silica, Phenoxyethanol, Disodium Ethylene Dicocamide PEG-15 Disulfate, Phenylpropanol, Panthenol, Calaguala ( Polypodium leucotomos ) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea ( Camellia sinensis ) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Tocopheryl Acetate, Steareth-21, Steareth-2, Triethoxycaprylylsilane, BHT, Citric Acid, Disodium EDTA, Fragrance, Linalool, Synthetic Iron Oxide* (CI 77491, CI 77492, CI 77499). * Contains one or more of these ingredients.

NDCs 82141-2340-1 & 82141-2341-1 Water, Butylene Glycol Cocoate,Hexylene Glycol, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Styrene/Acrylates Copolymer, Ceteareth-25, Propylene Glycol, Dipropylene Glycol Dibenzoate, Silica, Phenoxyethanol, Phenylpropanol, Disodium Ethylene Dicocamide PEG-15 Disulfate, Panthenol, Calaguala ( Polypodium leucotomos ) Leaf Extract, Sodium Hyaluronate, Caprylyl Glycol, Mica, Tea ( Camellia sinensis ) Leaf Extract, Propanediol, PPG-15 Stearyl Ether Benzoate, Tocopheryl Acetate, Glyceryl Steara…

🎯 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 ↗
← 82141-2327-01 · Chipican 82141-2329-01 · Chipican →
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.