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CLARINS - MULTI-INTENSIVE JOUR SUPER RESTORATIVE DAY BROAD SPECTRUM - SPF 15 - SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL Cream, 50 mL — NDC 58668-9920-1 (Billing 58668-9920-01)

by Laboratoires Clarins · 50 mL in 1 JAR

This is a package of 50 mL of CLARINS - MULTI-INTENSIVE JOUR SUPER RESTORATIVE DAY BROAD SPECTRUM - SPF 15 - SUNSCREEN AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL Cream from Laboratoires Clarins, marketed since Apr 2023 and currently FDA-listed. It is this product's only package size.

NDC 58668-9920-01
🏷️ FDA NDC (as labeled) 58668-9920-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 58668-9920-1
Product NDC 58668-9920
11-digit billing NDC 58668992001
UNII G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM
Application # M020
SPL Set ID 157cb8ca-1a36-41fb-be9e-b157b146dc4d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-04-01
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 58668-9920-1 — 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 → 58668-9920-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is a topical cream sunscreen marketed as an over-the-counter product under FDA's OTC monograph rules. It contains four UV-absorbing ingredients (avobenzone, homosalate, octisalate, and octocrylene) that are typically used together to filter ultraviolet radiation and help protect skin from sun exposure. The product is labeled as broad-spectrum SPF 15, meaning it is formulated to block both UVA and UVB rays. This is a cosmetic-grade moisturizer combined with sunscreen actives intended for daily facial use.

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
58668-9920-01 You're viewing this Main listing 50 mL in 1 JAR 2023-04-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
CVS Health SPF 30 Ultra Protection 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL 51316-0025-11 CVS 237 ml — — FDA listed —
Fruit of the Earth Sun Town City SPF 30 Sunscreen 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL 62217-0079-11 Fruit 237 ml — — FDA listed —
TopCare Everyday Sport Sun Broad Spectrum SPF 30 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL 36800-0280-11 TOPCO 237 ml — — FDA listed —
Walgreens SPF 30 Sport 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL 00363-0093-09 WALGREEN 89 ml — — FDA listed —
Wegmans SPORT BROAD SPECTRUM SPF 30 SUNSCREEN 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mL 47124-0123-11 WEGMANS 237 ml — — FDA listed —
Clarins - Multi-Intensive Jour Super Restorative Day Broad Spectrum - Spf 15 - Sunscreen 30 mg/mL; 80 mg/mL; 45 mg/mL; 60 mg/mLthis 58668-9920-01 Laboratoires 50 ml — — 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
Apr 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerLaboratoires Clarins
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code58668
First marketedApr 2023
Product typeHuman Otc Drug
Portfolio14 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.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

Uses: • helps prevent sunburn • if used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun Directions

⏱️ Dosage and Administration 107 words ▾

Directions: • apply liberally 15 minutes before sun exposure • apply to all skin exposed to the sun • children under 6 months: Ask a doctor • Spending time in the sun in creases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m. – 2 p.m. • wear long-sleeved shirts, pants, hats and sunglasses • reapply at least every 2 hours • use a water resistant sun screen if swimming or sweating Sun Protection Measures.

⚠️ Warnings 60 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. Keep out of reach of children. If product is swallowed, get me dical help or contact a Poison Control Center right away.

🧪 Active Ingredient 12 words ▾

Active ingredients AVOBENZONE 3% HOMOSALATE 8% OCTISALATE 4.5% OCTOCRYLENE 6% Purpose Sunscreen

🧪 Inactive Ingredients 166 words ▾

Inactive ingredients: AQUA/WATER/EAU . DICAPRYLYL CARBONATE . GLYCERIN .

BUTYLOCTYL SALICYLATE . PENTYLENE GLYCOL . CETEARYL ALCOHOL .

ASCORBYL GLUCOSIDE . POTASSIUM CETYL PHOSPHATE . SQUALANE .

DIMETHICONE . PARFUM/FRAGRANCE . BUTYLENE GLYCOL .

CETEARYL GLUCOSIDE . ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER . SODIUM HYDROXIDE .

XYLITYLGLUCOSIDE . HYDROXYACETOPHENONE . SODIUM CITRATE .

ANHYDROXYLITOL . ETHYLHEXYLGLYCERIN . TOCOPHERYL ACETATE .

XANTHAN GUM . CI 77891/TITANIUM DIOXIDE . CAPRYLIC/CAPRIC TRIGLYCERIDE .

SYNTHETIC FLUORPHLOGOPITE . DIMETHICONOL . XYLITOL .

DISODIUM EDTA . SODIUM LACTATE . SUCROSE PALMITATE .

GLUCOSE . CARBOMER . CITRIC ACID .

HARUNGANA MADAGASCARIENSIS EXTRACT . MARRUBIUM VULGARE EXTRACT . COCO-GLUCOSIDE .

BALANITES ROXBURGHII SEED OIL . GLYCERYL LINOLEATE . PHENETHYL ALCOHOL .

FURCELLARIA LUMBRICALIS EXTRACT . PANCRATIUM MARITIMUM EXTRACT . TIN OXIDE .

ULEX EUROPAEUS LEAF/ROOT/STEM EXTRACT . TOCOPHEROL . POTASSIUM SORBATE .

PROPANEDIOL . PECTIN . SODIUM HYALURONATE .

GUAR HYDROXYPROPYLTRIMO- NIUM CHLORIDE . CI 14700/RED 4 . PALMITOYL TRIPEPTIDE-1 .

LAPSANA COMMUNIS FLOWER/LEAF/STEM EXTRACT . MARIS SAL/SEA SALT/SEL MARIN . PALMITOYL TETRAPEPTIDE-7. [S4041A]

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 9 words ▾

Do not use • on damaged or broken skin.

📄 When Using This Product 14 words ▾

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

📄 Stop Use and Ask a Doctor If 10 words ▾

Stop use and ask a doctor if • rash occurs.

📄 Keep Out of Reach of Children 22 words ▾

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

📄 Questions or Comments 12 words ▾

Questions or comments? Call 1-866-325-2746 Monday-Friday 9 a.m. to 6:30 p.m. ET

📄 Package Label / Principal Display Panel 8 words ▾

Package Labeling: Outer Package Inner Label0 Box Box2

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE — the ingredient across all brands.

Top reported reactions

Rash40
Skin Cancer39
Pruritus31
Erythema26
Pain26
Dyspnoea25
Fatigue25

Age at onset

Infant1
Child6
Adolescent4
Adult61
Elderly45

Reporter sex

650 reports
Male · 36%
Female · 64%

Serious outcomes

Hospitalization99
Disabling23
Death23
Life-threatening11
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 57 7
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.

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Laboratoires Clarins. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Laboratoires Clarins 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.
← 58668-9918-01 · Laboratoires 58668-9921-01 · Laboratoires →
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.