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NARS PURE RADIANT TINTED MOISTURIZER Granada OCTINOXATE, TITANIUM DIOXIDE 4.044 g/50mL; 3.996 g/50mL Cream — NDC 13734-0192-60 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

NARS PURE RADIANT TINTED MOISTURIZER Granada OCTINOXATE, TITANIUM DIOXIDE 4.044 g/50mL; 3.996 g/50mL Cream — NDC 13734-192-60 (Billing 13734-0192-60)

by NARS Cosmetics · 1 TUBE in 1 BOX / 50 mL in 1 TUBE

This is a package of NARS PURE RADIANT TINTED MOISTURIZER Granada OCTINOXATE, TITANIUM DIOXIDE 4.044 g/50mL; 3.996 g/50mL Cream from NARS Cosmetics, marketed since Apr 2021 and currently FDA-listed. It is this product's only package size.

NDC 13734-0192-60
🏷️ FDA NDC (as labeled) 13734-192-60 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 20, 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 13734-192-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
13734 labeler · 192 product · 60 package
Package marketed since
Dec 17, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 1373419260 7
FDA record last changed
Aug 20, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 13734-192-60
Product NDC 13734-192
11-digit billing NDC 13734019260
UNII 4Y5P7MUD51, 15FIX9V2JP
Application # M020
SPL Set ID 5bb5d035-16d9-4843-b9aa-d30730c88508
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-04-01
Route TOPICAL
Dosage form CREAM
Substance OCTINOXATE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 13734-192-60 — 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 → 13734-0192-60. 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?

NARS Pure Radiant Tinted Moisturizer Granada is a topical cream containing octinoxate and titanium dioxide, which are active ingredients commonly used as ultraviolet (UV) filters in sunscreen products. This tinted moisturizer is marketed as an over-the-counter monograph drug, meaning it is formulated according to FDA's established rules for sunscreen products rather than as an individually reviewed application. The combination of these UV-filtering ingredients is typically included to help protect skin from sun exposure.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
13734-0192-60 You're viewing this Main listing 1 TUBE in 1 BOX / 50 mL in 1 TUBE 2025-12-17 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
NARS PURE RADIANT TINTED MOISTURIZER Cuzco 4.044 g/50mL; 3.996 g/50mL 13734-0177-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Marrakesh 4.044 g/50mL; 3.996 g/50mL 13734-0188-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Gotland 4.044 g/50mL; 3.996 g/50mL 13734-0183-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Guernsey 4.044 g/50mL; 3.996 g/50mL 13734-0191-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Finland 4.044 g/50mL; 3.996 g/50mL 13734-0181-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Granada 4.044 g/50mL; 3.996 g/50mLthis 13734-0192-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Auckland 4.044 g/50mL; 3.996 g/50mL 13734-0187-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Mykonos 4.044 g/50mL; 3.996 g/50mL 13734-0185-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Norwich 4.044 g/50mL; 3.996 g/50mL 13734-0184-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Groenland 4.044 g/50mL; 3.996 g/50mL 13734-0179-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Alaska 4.044 g/50mL; 3.996 g/50mL 13734-0180-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Santiago 4.044 g/50mL; 3.996 g/50mL 13734-0189-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER St. Moritz 4.044 g/50mL; 3.996 g/50mL 13734-0178-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Terre Neuve 4.044 g/50mL; 3.996 g/50mL 13734-0182-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Havana 4.044 g/50mL; 3.996 g/50mL 13734-0190-60 NARS 1 tube — — FDA listed —
NARS PURE RADIANT TINTED MOISTURIZER Sydney 4.044 g/50mL; 3.996 g/50mL 13734-0186-60 NARS 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

🏛️
2021
On the market since
Apr 2021
📍
2026
Currently FDA-listed
5 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.

What it looks like

Color brown
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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII BPX036043D
    A naturally derived substance from marine bacteria, used in some formulations as a preservative or antimicrobial agent to help protect the medicine from contamination during storage.
  • 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 2V52R0NHXW
    Ascorbyl glucoside is a stable form of vitamin C derived from ascorbic acid and glucose. It functions as an antioxidant in medicines to protect other ingredients from breaking down when exposed to air or light.
  • 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 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.
  • UNII 69W9UMG3P8
    A synthetic oily compound used as a plasticizer and solvent in medicines. It helps soften and improve flexibility of coatings on tablets and capsules, and aids in dissolving or dispersing active ingredients in liquid formulations.
  • 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 H895X08VNQ
    A silicone-based polymer that forms small, hard particles. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII I445L28B12
    A silicone-based compound that acts as a lubricant and glidant in tablet and capsule formulations. It reduces friction between particles and on equipment surfaces, helping medicines flow smoothly during manufacturing and tablet compression.
  • 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 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 446U8J075B
    Nylon-12 is a synthetic plastic polymer used as a coating or film-forming agent in medicines. It helps create a protective barrier around tablets or capsules to control how and when the medicine is released in the body.
  • 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 TYP81E471F
    A silicone-based lubricant and anti-foaming agent derived from dimethicone, a synthetic polymer. It helps reduce friction during tablet or capsule manufacturing and prevents excessive foam in liquid formulations.
  • 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 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 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 87GE52P74G
    Sea salt is sodium chloride harvested from seawater. It acts as a flavoring agent and preservative in medications, helping enhance taste and prevent microbial growth.
  • UNII 4VON5FNS3C
    Sodium metabisulfite is a preservative derived from sulfur compounds. It prevents microbial growth and oxidation in medicines, helping extend shelf life and maintain product stability.
  • UNII VU97D01BF9
    A waxy emulsifier derived from sorbitol, a natural sugar alcohol. It helps blend oil and water-based ingredients together and improves the texture and stability of the medicine.
  • 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 R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII 420IP921MB
    A chelating agent derived from edetic acid that binds to metals in the formulation. It helps stabilize the medicine by preventing metal ions from causing breakdown or discoloration.
  • 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.

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

The official label also statesWATER • DIMETHICONE • BUTYLENE GLYCOL • GLYCERIN • PROPANEDIOL • DIETHYLHEXYL SUCCINATE • NYLON-12 • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • PEG-10 DIMETHICONE • ALUMINUM HYDROXIDE • DIPHENYLSILOXY PHENYL TRIMETHICONE • DISTEARDIMONIUM HECTORITE • SORBITAN SESQUIISOSTEARATE • POLYMETHYLSILSESQUIOXANE • TRISODIUM EDTA • ASCORBYL GLUCOSIDE • POLYSILICONE-2 • ALTEROMONAS FERMENT EXTRACT • BHT • SODIUM METABISULFITE • CURCUMA LONGA (TURMERIC) ROOT EXTRACT • STEARIC ACID • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • FRAGRANCE • TOCOPHEROL • VIBRIO ALGINOLYTICUS FERMENT FILTRATE • SEA SALT • PHENOXYETHANOL • [MAY CONTAIN: TITANIUM DIOXIDE • IRON OXIDES] •

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.

Manufacturer & labeler

LabelerNARS Cosmetics
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code13734
First marketedApr 2021
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from NARS Cosmetics labeler code 13734

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 📦 Storage and Handling 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Uses helps prevent sunbun 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 For sunscreen use: apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours 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 or higher and other sun protection mesures including: • limit time in the sun, especially from 10 a.m. - 2 p.m. • wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months: Ask a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 14 words ▾

Other information Protect this product in this container from excessive heat and direct sun

🧪 Inactive Ingredients 90 words ▾

WATER • DIMETHICONE • BUTYLENE GLYCOL • GLYCERIN • PROPANEDIOL • DIETHYLHEXYL SUCCINATE • NYLON-12 • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • PEG-10 DIMETHICONE • ALUMINUM HYDROXIDE • DIPHENYLSILOXY PHENYL TRIMETHICONE • DISTEARDIMONIUM HECTORITE • SORBITAN SESQUIISOSTEARATE • POLYMETHYLSILSESQUIOXANE • TRISODIUM EDTA • ASCORBYL GLUCOSIDE • POLYSILICONE-2 • ALTEROMONAS FERMENT EXTRACT • BHT • SODIUM METABISULFITE • CURCUMA LONGA (TURMERIC) ROOT EXTRACT • STEARIC ACID • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • FRAGRANCE • TOCOPHEROL • VIBRIO ALGINOLYTICUS FERMENT FILTRATE • SEA SALT • PHENOXYETHANOL • [MAY CONTAIN: TITANIUM DIOXIDE • IRON OXIDES] •

🎯 Purpose 10 words ▾

Active Ingredients Purpose Octinoxate 6.74% Sunscreen Titanium Dioxide 6.66% Sunscreen

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin

📄 When Using This Product 13 words ▾

When using this product keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 7 words ▾

Questions or comments? Call toll free 1-888-788-NARS

📄 Package Label / Principal Display Panel ~2 min read ▾

PRINCIPLE DISPLAY PANEL - 50 mL Tube Cuzco NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Cuzco

PRINCIPLE DISPLAY PANEL - 50 mL Tube St. Moritz NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL St Moritz

PRINCIPLE DISPLAY PANEL - 50 mL Tube Groenland NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Groenland

PRINCIPLE DISPLAY PANEL - 50 mL Tube Alaska NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Alaska

PRINCIPLE DISPLAY PANEL - 50 mL Tube Finland NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Finland

PRINCIPLE DISPLAY PANEL - 50 mL Tube Terre Neuve NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Terre Neuve

PRINCIPLE DISPLAY PANEL - 50 mL Tube Gotland NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Gotland

PRINCIPLE DISPLAY PANEL - 50 mL Tube Norwich NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT. 1.9 oz. 50 mL Norwich

PRINCIPLE DISPLAY PANEL - 50 mL Tube Mykonos NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Mykonos

PRINCIPLE DISPLAY PANEL - 50 mL Tube Sydney NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Sydney

PRINCIPLE DISPLAY PANEL - 50 mL Tube Auckland NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Auckland

PRINCIPLE DISPLAY PANEL - 50 mL Tube Marrakesh NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Marrakesh

PRINCIPLE DISPLAY PANEL - 50 mL Tube Santiago NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Santiago

PRINCIPLE DISPLAY PANEL - 50 mL Tube Havana NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Havana

PRINCIPLE DISPLAY PANEL - 50 mL Tube Guernsey NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Gurernsey

PRINCIPLE DISPLAY PANEL - 50 mL Tube Granada NARS PURE RADIANT TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN NET WT.

1.9Oz. 50 mL Granada

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
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 NARS Cosmetics. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
NARS Cosmetics 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.
← 13734-0191-60 · NARS 13746-0102-01 · Srikem →
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.