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No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Cedar Octinoxate, Titanium Dioxide 2.1 g/30g; .51 g/30g Cream

by BCM Cosmetique SAS · 1 BOTTLE in 1 CARTON (61589-9541-1) / 30 g in 1 BOTTLE
NDC 61589-9541-01
🏷️ FDA NDC (as labeled) 61589-9541-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 61589-9541-1
Product NDC 61589-9541
11-digit billing NDC 61589954101
UNII 4Y5P7MUD51, 15FIX9V2JP
Application # M020
SPL Set ID 970571f9-3d6b-46ae-a668-745de1911fa2
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-11-09
Route TOPICAL
Dosage form CREAM
Substance OCTINOXATE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 61589-9541-1 — 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 → 61589-9541-01. 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

LabelerBCM Cosmetique SAS
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code61589
First marketedNov 2021
Product typeHuman Otc Drug
Portfolio72 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 topical cream sunscreen marketed as an over-the-counter monograph product under FDA regulation. It contains two active ingredients that function as ultraviolet (UV) filters: octinoxate and titanium dioxide. These ingredients are commonly used together in sunscreen products to help protect skin from UVA and UVB radiation. The product is formulated as a foundation serum with a stated broad spectrum sun protection factor of 20.

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.

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.

💲 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
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Cool Beige 2.1 g/30g; .51 g/30g 61589-9531-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Wheat 2.1 g/30g; .51 g/30g 61589-9533-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Umber 2.1 g/30g; .51 g/30g 61589-9542-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Cool Vanilla 2.1 g/30g; .51 g/30g 61589-9527-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Bamboo 2.1 g/30g; .51 g/30g 61589-9537-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Porcelain 2.1 g/30g; .51 g/30g 61589-9525-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Tawny 2.1 g/30g; .51 g/30g 61589-9535-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Cedar 2.1 g/30g; .51 g/30gthis 61589-9541-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Warm Ivory 2.1 g/30g; .51 g/30g 61589-9528-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Hazelnut 2.1 g/30g; .51 g/30g 61589-9539-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Honey 2.1 g/30g; .51 g/30g 61589-9532-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Latte 2.1 g/30g; .51 g/30g 61589-9534-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Chestnut 2.1 g/30g; .51 g/30g 61589-9540-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Calico 2.1 g/30g; .51 g/30g 61589-9526-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Cool Ivory 2.1 g/30g; .51 g/30g 61589-9529-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Warm Beige 2.1 g/30g; .51 g/30g 61589-9530-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Dune 2.1 g/30g; .51 g/30g 61589-9536-01 BCM 1 bottle — — FDA listed —
No7 Restore and Renew Multi Action Serum Foundation Sunscreen Broad Spectrum SPF 20 Amber 2.1 g/30g; .51 g/30g 61589-9538-01 BCM 1 bottle — — 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
Nov 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.

🔬 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 Octinoxate, Titanium Dioxide — the ingredient across all brands.

Top reported reactions

Dermatitis Contact1
Emotional Distress1
Hyperaesthesia1
Hypersensitivity1
Product Formulation Issue1
Rash1
Self Esteem Decreased1

Reporter sex

2 reports
Female · 100%
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
61589-9541-01 You're viewing this 1 BOTTLE in 1 CARTON (61589-9541-1) / 30 g in 1 BOTTLE 2021-11-09 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 — 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 FDA registers it as 61589-9541-1, 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: 61589-9541-01, written without dashes as 61589954101. 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 61589-9541-01, the first segment (61589) is the labeler code FDA assigned to BCM Cosmetique SAS; the middle segment (9541) 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 BCM Cosmetique SAS. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
BCM Cosmetique SAS 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 and Cautions ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description 💬 Information for Patients
🎯 Indications and Usage 97 words ▾

Directions Directions for suncreen use apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating children under 6 months of age: 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

⏱️ Dosage and Administration 97 words ▾

Directions Directions for suncreen use apply liberally 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating children under 6 months of age: 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 and Cautions 26 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

⚠️ Warnings 26 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

📦 Storage and Handling 14 words ▾

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

🧪 Active Ingredient 11 words ▾

Carton Active Ingredients Section Active Ingredients Octinoxate 7% Titanium dioxide 1.7%

🧪 Inactive Ingredients 117 words ▾

Inactive ingredients Aqua (Water), Caprylyl methicone, Dimethicone, Ethylhexyl methoxycinnamate, Phenyl trimethicone, Glycerin, Mica, trimethylsiloxysilicate, Butylene glycol, Silica, PEG-9 dimethicone, Titanium dioxide (nano), Bis-isobutyl PEF/PPG-10/7/dimethicone copolymer, Disteardimonium hectorite, Magnesium sulfate, Phenoxyethanol, Alcohol denate., Triethyl citrate, Panthenol, Triethoxycaprylylsilane, Pentylene glycol, Caprylyl glycol, Propylene glycol, Tocopheryl acetate, Ascorbyl glucoside, Hibiscus abelmoschus extract, Retinyl palmitate, Ethylhexylglycerin, Tetrasodium EDTA, Sorbitan laurate, Panax ginseng root extract, Sodium lauroyl lactylate, Carbomer, Polysorbate 20, Potassium hydroxide, Dimethylmethoxy chromanol, Hydroxyethylcellulose, Xanthan gum, 3-Aminopropane sulfonic acid, Calcium hydroxymethionine, Acetyl dipeptide-1 cetyl ester, BHT, Morus alba leaf extract, Ceramide NP, Ceramide AP, Phytosphingosine, Cholesterol, Tocopherol, Palmitoyl tripeptide-1, Palmitoyl tetrapeptide-7, Ceramide EOP, [+/- CI 77891 (Titanium dioxide), CI 77492 (Iron oxides), CI 77491 (Iron oxides), CI 77499 (Iron oxides)].

🎯 Purpose 6 words ▾

Uses Uses - helps prevent sunburn

📋 Description 169 words ▾

No7 Restore & Renew MULTI ACTION Serum Foundation Visibly conceals the 5 key signs of ageing LIGHT - MEDIUM COVERAGE 30 ml e 1 US Fl. Oz. Tackle the advanced signs of aging with our multi-tasking, age-defying foundation.

Enriched with No7 Restore & Renew MULTI ACTION technology: MATRIXYL 3000 PLUS and Firming & Brightening Complexes, it visibly improves the 5 key signs of aging by instantly concealing fine lines & wrinkles, age spots, uneven texture & tone, with skin appearing lifted and firmer over time*. A light - medium, buildable coverage that gently glides on and blends seamlessly. The Flexible Formula moves in harmony with your facial expressions throughout the day, ensuring the foundation doesn't migrate into lnes or wrinkles.

SPF 20 helps to actively protect skin from the damaging effects of the sun. For best results blend on smoothyl and evenly with your fingers, sponge or brush. Use on top of your regular Restore & Renew regime to superchage your results.

Suitable for sensitive skin. *whilst wearing foundation

💬 Information for Patients 13 words ▾

Information Made in France Boots Retail USA Dist. New York, NY 10005 www.No7beauty.com

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61589-9540-01 · BCM 61589-9542-01 · BCM →
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.