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

by BCM Cosmetique SAS · 1 BOTTLE in 1 CARTON (61589-9540-1) / 30 g in 1 BOTTLE
NDC 61589-9540-01
🏷️ FDA NDC (as labeled) 61589-9540-1 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) 61589-9540-1
Product NDC 61589-9540
11-digit billing NDC 61589954001
UNII 4Y5P7MUD51, 15FIX9V2JP
Application # M020
SPL Set ID 6a44f926-11b4-4bc4-8d5d-721a89c4f0cc
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 61589-9540-1 — 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 → 61589-9540-01. 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 that combines two active ingredients to help protect skin from ultraviolet (UV) radiation. Octinoxate and titanium dioxide are both UV filters commonly used in sunscreen products to absorb and reflect UV rays from the sun. The product is formulated as an over-the-counter monograph drug, meaning it follows the FDA's established rules for sunscreen ingredients and strengths rather than being individually reviewed. It is intended for application to the 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 599O6K8K81
    A plant extract from the musk mallow flower, used as a natural flavoring agent and fragrance ingredient to add pleasant taste and scent to the medicine.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 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 Q95M2P1KJL
    A silicone-based ingredient that acts as a lubricant and glidant. It helps the tablet or capsule move smoothly through manufacturing equipment and improves powder flow during production.
  • UNII 4Q93RCW27E
    A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII 88KCS7120E
    Ceramide 9 is a fatty lipid found naturally in skin. It's used in medicines as an emollient and skin-conditioning agent to help soften and protect the skin barrier in topical formulations.
  • UNII F1X8L2B00J
    A naturally derived fatty substance that helps bind and condition the product's texture. It works as an emollient and skin-conditioning agent in topical formulations, helping maintain moisture and smoothness.
  • UNII 97C5T2UQ7J
    Cholesterol is a fatty substance found naturally in animal tissues. In medications, it's used as an ingredient in liposomal formulations and lipid-based drug delivery systems to help encapsulate and stabilize active drugs for better absorption.
  • UNII 1VK0YS654L
    Desmeninol calcium is a calcium-derived compound used as a buffering and stabilizing agent in medications. It helps maintain the proper pH and shelf stability of the drug product.
  • 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 XBH432G01F
    A synthetic antioxidant compound used to prevent oxidation and degradation of the active ingredients and other components in the medicine, helping maintain its stability and shelf life.
  • 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 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII CZZ9T1T1X4
    A mineral salt compound used in some medications as a chelating agent and calcium regulator. It helps stabilize the formulation and prevent mineral buildup that could interfere with the medicine's effectiveness or shelf life.
  • 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 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 T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • 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 M8YIA49Q2P
    Morus alba leaf is a plant-derived ingredient used in some formulations as a natural filler and potential thickening agent. It may help give the product body and texture.
  • UNII HA41Z1UF8D
    N-acetyl dipeptide-1 is a synthetic compound made from two linked amino acids with an acetyl group attached. It functions as a skin-conditioning agent and emollient in topical formulations to help soften and smooth the skin surface.
  • UNII Y5DC3IN066
    A buffering agent derived from amino acids and sulfonic acid. It helps maintain stable pH levels in liquid medications to keep the medicine effective and prevent degradation during storage.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • UNII P9T4K47OM0
    A plant extract from Asian ginseng root. Used as a flavor ingredient and to add aroma to the medicine.
  • 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 9OZ27X065D
    A silicone-based compound combined with polyethylene glycol. It acts as an emulsifier and surfactant, helping oils and water mix smoothly in liquid or semi-solid medicines, and improves how the product spreads and feels.
  • UNII 5GDV42659J
    A silicone-based substance combined with polyethylene glycol and polypropylene glycol. It acts as an emulsifier and surfactant to help mix oil and water components, and improves how the medicine spreads or flows during manufacturing and use.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • 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 DR0K5NOJ4R
    Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
  • UNII GIN46U9Q2Q
    Phytosphingosine is a naturally derived fatty compound that helps stabilize and thicken skincare and cosmetic formulations. It works as an emollient and conditioning agent to improve texture and skin feel in topical products.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • 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 7243K85WFO
    Sodium lauroyl lactylate is a mild surfactant derived from natural fats and lactic acid. It acts as an emulsifier and solubilizer to help blend oil and water-based ingredients and improve how the body absorbs the active drug.
  • UNII 6W9PS8B71J
    Sorbitan monolaurate is a natural oil-derived emulsifier made from sorbitol and lauric acid. It helps mix oils and water-based ingredients together in the medicine so the formula stays uniform and smooth.
  • 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 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.
  • UNII 8Z96QXD6UM
    Triethyl citrate is a clear liquid derived from citric acid. It acts as a plasticizer and solvent in tablet coatings and film formulations, helping the coating remain flexible and adhere properly to the medicine.
  • UNII 5041RX63GN
    A synthetic silicon-based polymer used as a glidant and anti-caking agent. It helps powder particles flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesAqua (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)].

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
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/30g 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/30gthis 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%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2 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
61589-9540-01 You're viewing this 1 BOTTLE in 1 CARTON (61589-9540-1) / 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) ✓ 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 61589-9540-1, 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: 61589-9540-01, written without dashes as 61589954001. 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 61589-9540-01, the first segment (61589) is the labeler code FDA assigned to BCM Cosmetique SAS; the middle segment (9540) 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 ↗
← 61589-9539-01 · BCM 61589-9541-01 · 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.