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BB blur tinted moisturizer Broad Spectrum SPF 30 light Titanium Dioxide and Zinc Oxide 45.5 mg/mL; 35 mg/mL Liquid — NDC 51060-0365-01 package photo

BB blur tinted moisturizer Broad Spectrum SPF 30 light Titanium Dioxide and Zinc Oxide 45.5 mg/mL; 35 mg/mL Liquid

by Tarte, Inc. · 1 TUBE in 1 CARTON (51060-365-01) / 30 mL in 1 TUBE
NDC 51060-0365-01
🏷️ FDA NDC (as labeled) 51060-365-01 billing pads the product 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

🆔 Identity & classification

FDA NDC (as labeled) 51060-365-01
Product NDC 51060-365
11-digit billing NDC 51060036501
UNII SOI2LOH54Z, 15FIX9V2JP
Application # M020
SPL Set ID 207aaa0c-777f-4abd-96b7-64666eb87f53
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-05-01
Route TOPICAL
Dosage form LIQUID
Substance TITANIUM DIOXIDE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 51060-365-01 — 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 → 51060-0365-01. 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

LabelerTarte, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code51060
First marketedMay 2023
Product typeHuman Otc Drug
Portfolio85 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 a tinted liquid moisturizer applied to the skin that contains titanium dioxide and zinc oxide as active ingredients. Both minerals function as physical sunscreen filters, reflecting and scattering ultraviolet light to help protect skin from sun damage. The product is classified as an over-the-counter monograph drug, meaning it follows FDA's established safety and effectiveness rules for sunscreen products. It is typically used as a daily facial product that combines moisturizing and broad-spectrum sun protection.

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 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 E24GX49LD8
    A synthetic organic compound used in pharmaceuticals as a preservative and antimicrobial agent. It helps prevent contamination and extends shelf life in liquid and topical formulations.
  • UNII V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • 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 6GRV67N0U2
    Diamond powder is a finely ground form of crystalline carbon. It's used in some formulations as a polishing or abrasive agent, and occasionally as a colorant or for texture in solid dosage forms.
  • UNII 9E4CO0W6C5
    A silicone-based polymer that forms soft, spongy particles. Used as a texture modifier and suspending agent to improve how the product feels and flows, and to help keep ingredients evenly distributed throughout the formulation.
  • UNII E6AHA53N1H
    A synthetic amino acid derivative used as a skin-conditioning agent and emollient in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • 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 4CG9F9W01Q
    A synthetic fatty acid ester used as an emollient and skin-conditioning agent in topical medicines. It helps soften the product texture and improves how it spreads and absorbs into the skin.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • 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 8PR7V1SVM0
    A silicone-based lubricant combined with polyethylene glycol. It reduces friction and helps the medicine flow smoothly during manufacturing and improves how the product feels when applied or swallowed.
  • UNII 820DPX33S7
    A synthetic emulsifier derived from glycerin and fatty acids. It helps mix oil and water-based ingredients together and keeps them evenly blended throughout the product.
  • UNII Z570VEV8XK
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles so the medicine flows smoothly during manufacturing and remains free-flowing in the bottle.
  • 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.

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

The official label also statesCyclopentasiloxane, isododecane, mica, polysilicone-11, polymethylsilsesquioxane, hexyl laurate, PEG-10 dimethicone, polyglyceryl-4 isostearate, stearic acid, cetyl PEG/PPG-10/1 dimethicone, alumina, triethoxycaprylylsilane, dipalmitoyl hydroxyproline, diamond powder, iron oxides. OX100FP000401.

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
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen fair 45.5 mg/mL; 35 mg/mL 51060-0311-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen light 45.5 mg/mL; 35 mg/mL 51060-0312-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen light-medium 45.5 mg/mL; 35 mg/mL 51060-0313-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen medium 45.5 mg/mL; 35 mg/mL 51060-0314-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen tan 45.5 mg/mL; 35 mg/mL 51060-0315-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen tan-deep 45.5 mg/mL; 35 mg/mL 51060-0316-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen deep 45.5 mg/mL; 35 mg/mL 51060-0317-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen rich 45.5 mg/mL; 35 mg/mL 51060-0318-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen mahogany 45.5 mg/mL; 35 mg/mL 51060-0319-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen light 45.5 mg/mL; 35 mg/mL 51060-0320-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen medium 45.5 mg/mL; 35 mg/mL 51060-0321-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen tan 45.5 mg/mL; 35 mg/mL 51060-0322-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen deep 45.5 mg/mL; 35 mg/mL 51060-0323-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 light 45.5 mg/mL; 35 mg/mLthis 51060-0365-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 medium 45.5 mg/mL; 35 mg/mL 51060-0366-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 medium-tan 45.5 mg/mL; 35 mg/mL 51060-0367-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 tan 45.5 mg/mL; 35 mg/mL 51060-0368-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 tan deep 45.5 mg/mL; 35 mg/mL 51060-0369-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 deep 45.5 mg/mL; 35 mg/mL 51060-0370-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 rich 45.5 mg/mL; 35 mg/mL 51060-0371-01 Tarte, 1 tube — — FDA listed —
BB blur tinted moisturizer Broad Spectrum SPF 30 mahogany 45.5 mg/mL; 35 mg/mL 51060-0372-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen fair-light 45.5 mg/mL; 35 mg/mL 51060-0374-01 Tarte, 1 tube — — FDA listed —
sugar rush skin treat poreless tinted moisturizer Broad Spectrum SPF 20 Sunscreen medium-tan 45.5 mg/mL; 35 mg/mL 51060-0375-01 Tarte, 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

🏛️
2023
On the market since
May 2023
📍
2026
Currently FDA-listed
3 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
51060-0365-01 You're viewing this 1 TUBE in 1 CARTON (51060-365-01) / 30 mL in 1 TUBE 2023-05-01 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 51060-365-01, 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: 51060-0365-01, written without dashes as 51060036501. 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 51060-0365-01, the first segment (51060) is the labeler code FDA assigned to Tarte, Inc.; the middle segment (0365) 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 Tarte, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Tarte, Inc. 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 30 words ▾

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

⏱️ Dosage and Administration 95 words ▾

Directions Shake before use. Apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating.

Reapply at least every 2 hours. Children under 6 months: 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

⚠️ Warnings 54 words ▾

Warnings For external use only. Stop use and ask doctor if rash occurs. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 33 words ▾

Other information Protect the product in this container from excessive heat and direct sunlight. You may report a serious adverse reaction to: tarte c/o Report Reaction, LLC, P.O. Box 22, Plainsboro, NJ 08536-0222.

🧪 Active Ingredient 10 words ▾

Active Ingredients Titanium Dioxide 4.55% Sunscreen Zinc Oxide 3.5% Sunscreen

🧪 Inactive Ingredients 27 words ▾

Inactive Ingredients Cyclopentasiloxane, isododecane, mica, polysilicone-11, polymethylsilsesquioxane, hexyl laurate, PEG-10 dimethicone, polyglyceryl-4 isostearate, stearic acid, cetyl PEG/PPG-10/1 dimethicone, alumina, triethoxycaprylylsilane, dipalmitoyl hydroxyproline, diamond powder, iron oxides. OX100FP000401.

🎯 Purpose 10 words ▾

Active Ingredients Titanium Dioxide 4.55% Sunscreen Zinc Oxide 3.5% Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 51060-0358-01 · Tarte, 51060-0366-01 · Tarte, →
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.