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No7 Future Renew Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 Avobenzone, Octinoxate, Octisalate, Octocrylene .15 g/5g; .025 g/5g; .375 g/5g; .25 g/5g Cream

by BCM Cosmetique SAS · 1 TUBE in 1 CARTON (61589-9715-2) / 15 g in 1 TUBE (61589-9715-1)
NDC 61589-9715-02
🏷️ FDA NDC (as labeled) 61589-9715-2 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 61589-9715-2
Product NDC 61589-9715
11-digit billing NDC 61589971502
UNII G63QQF2NOX, 4Y5P7MUD51, 5A68WGF6WM, 4X49Y0596W
UPC 5000167381542
Application # M020
SPL Set ID 35129e6f-c6bd-a9f7-e063-6394a90ab0e4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-08-31
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OCTISALATE
Why two NDCs? The FDA registers this code as 61589-9715-2 — 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 → 61589-9715-02. 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 marketedAug 2023
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 sold over the counter as a sunscreen with an SPF of 25. It contains four active ingredients (avobenzone, octinoxate, octisalate, and octocrylene) that function as ultraviolet light filters, commonly used in sunscreen products to help protect skin from UV radiation. The product is formulated as an OTC monograph drug, meaning it is marketed under FDA's established rules for sunscreen products rather than through an individual drug application.

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 A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII W59H9296ZG
    A synthetic polymer made from acrylic compounds and vinylpyrrolidone. It works as a film-former and thickener in topical products, helping create a smooth texture and improve how the medication spreads on skin.
  • 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 N7YC58165T
    A synthetic polymer made from glycerin and sebacic acid, used as a film-former and binder in medications. It helps hold tablet or capsule ingredients together and may coat the product for controlled release.
  • 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 DSO12WL7AU
    A salt derived from citric acid, this ingredient acts as a buffer and pH regulator in medicines. It helps maintain stable acidity levels and may improve taste or aid preservation.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII F4K100DXP3
    Dibutyl adipate is a synthetic oily liquid derived from adipic acid. It serves as a plasticizer and solvent in medicines, helping softens coatings and improves flexibility so tablets and capsules don't crack or break.
  • 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 343C7U75XW
    Dimethiconol is a silicone-based fluid that acts as an anti-foaming agent and lubricant in medications. It reduces bubble formation during manufacturing and helps the medicine flow smoothly through equipment.
  • UNII E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • 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 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 YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • 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 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII Z6T2ETB7SH
    A synthetic peptide made from amino acids and palmitic acid. It acts as a conditioning agent or emollient to improve texture and skin feel in topical formulations.
  • UNII MJN3TLA2BW
    A synthetic peptide derived from amino acids. It functions as an emollient and skin-conditioning agent to help soften and smooth the product's texture and improve how it feels on skin.
  • 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 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 W19EIO0DBE
    A plant-derived emulsifier made from glycerin and fatty acids. It helps mix oil and water-based ingredients together and stabilizes the product's texture in creams, lotions, and other cosmetic or topical formulations.
  • UNII 03KCY6P7UT
    A waxy compound derived from cetyl alcohol and phosphoric acid. It acts as an emulsifier to help blend oil and water ingredients, and as a thickener to give the medicine its proper texture and consistency.
  • 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 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 K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII MD83SFE959
    A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
  • UNII 8OC9U7TQZ0
    Tribehenin is a waxy, plant-derived substance that acts as a lubricant and glidant in tablets and capsules. It helps the medicine flow smoothly during manufacturing and prevents sticking during production and packaging.
  • UNII 035MV9S1C3
    A plastic-like polymer made from two chemical compounds joined together. It acts as a binder and film-former in tablets and capsules, helping hold ingredients together and create a protective coating on the medicine's surface.
  • 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.

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

The official label also statesAqua (Water), Dibutyl adipate, Glycerin, Polyglyceryl-3 methylglucose distearate, VP/eicosene copolymer, Capryloyl glycerin/sebacic acid copolymer, Tribehenin, Niacinamide, Dimethicone, Ammonium acryloyldimethyltaurate/VP copolymer, Butyrospermum parkii (Shea) butter, Tocopheryl acetate, Phenoxyethanol, Panthenol, Potassium cetyl phosphate, Caprylyl glycol, Parfum (fragrance), Dimethiconol, Sodium Benzoate, Sodium Hyaluronate, Ethylhexylglycerin, Hydrolyzed rice protein, Propylene glycol, Dipropylene glycol, Ascorbyl glucoside, Citric acid, Tetrasodium EDTA, T-butyl alcohol, Propanediol, Pentylene Glycol, Decyl glucoside, Morus alba leaf extract, BHT, Palmitoyl tetrapeptide-94, Palmitoyl tetrapeptide-95

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 Future Renew Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 .15 g/5g; .025 g/5g; .375 g/5g; .25 g/5g 61589-9705-02 BCM 1 tube — — FDA listed —
No7 Future Renew Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 .15 g/5g; .025 g/5g; .375 g/5g; .25 g/5gthis 61589-9715-02 BCM 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2023
On the market since
Aug 2023
📍
2026
Currently FDA-listed
3 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
61589-9715-02 You're viewing this 1 TUBE in 1 CARTON (61589-9715-2) / 15 g in 1 TUBE (61589-9715-1) 2023-08-31 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 61589-9715-2, 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: 61589-9715-02, written without dashes as 61589971502. 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 61589-9715-02, the first segment (61589) is the labeler code FDA assigned to BCM Cosmetique SAS; the middle segment (9715) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 92 words ▾

Directions Directions 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 7 words ▾

Apply liberally 15 minutes before sun exposure

⚠️ 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 53 words ▾

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 swallowed get medical help or contact a Poison Control Centre right away

📦 Storage and Handling 19 words ▾

Storage Other information protect the product in this container from excessive heat and direct sun avoid contact with fabrics

🧪 Active Ingredient 14 words ▾

Carton Active Ingredients Section Active ingredients Avobenzone 3% Octinoxate 0.5% Octisalate 5% Octocrylene 7.5%

🧪 Inactive Ingredients 72 words ▾

Inactive ingredients Aqua (Water), Dibutyl adipate, Glycerin, Polyglyceryl-3 methylglucose distearate, VP/eicosene copolymer, Capryloyl glycerin/sebacic acid copolymer, Tribehenin, Niacinamide, Dimethicone, Ammonium acryloyldimethyltaurate/VP copolymer, Butyrospermum parkii (Shea) butter, Tocopheryl acetate, Phenoxyethanol, Panthenol, Potassium cetyl phosphate, Caprylyl glycol, Parfum (fragrance), Dimethiconol, Sodium Benzoate, Sodium Hyaluronate, Ethylhexylglycerin, Hydrolyzed rice protein, Propylene glycol, Dipropylene glycol, Ascorbyl glucoside, Citric acid, Tetrasodium EDTA, T-butyl alcohol, Propanediol, Pentylene Glycol, Decyl glucoside, Morus alba leaf extract, BHT, Palmitoyl tetrapeptide-94, Palmitoyl tetrapeptide-95

🎯 Purpose 6 words ▾

Uses Uses - helps prevent sunburn

📋 Description 85 words ▾

Description No7 Future Renew TM Damage Reversal Day Cream Sunscreen Broad Spectrum SPF 25 Targets and helps prevent visible signs of skin damage 5 ml e .16 US Fl. Oz. Powered by PEPTICOLOY TM , No7's exclusive Peptide innovation, developed by world-leading scientists.

This cutting-edge, patent-pending technology supports skin's natural self-repair. Dermatologist approved For best results: Use every morning, massage in small upward circles over your face & neck. Proven to protect against UV and reverse visible signs of skin damage Suitable for Sensitive Skin

💬 Information for Patients 35 words ▾

USA: Questions? 1-866-75-BOOTS The Boots Company PLC Nottingham England NG2 3AA Boots Retail Ireland Dublin 12 Ireland Dist. in the USA by Boots Retail USA Inc. New York NY 10007 Made in the UK www.no7beauty.com

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 61589-9705-02 · BCM 61589-9720-02 · 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.