Home › NDC Lookup › Ingredients › Homosalate, Titanium Dioxide, Zinc Oxide › 72407-0430-40
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Deep homosalate, titanium dioxide, zinc oxide 7 g/100mL; 5.09 g/100mL; 9.5 g/100mL Cream — NDC 72407-0430-40 package photo

Ageless Glow Serum BB Cream Sunscreen SPF 40 - Deep homosalate, titanium dioxide, zinc oxide 7 g/100mL; 5.09 g/100mL; 9.5 g/100mL Cream

by Pur-lisse Beauty, LLC · 1 TUBE in 1 CARTON (72407-430-40) / 40 mL in 1 TUBE
NDC 72407-0430-40
🏷️ FDA NDC (as labeled) 72407-430-40 billing pads the product 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) 72407-430-40
Product NDC 72407-430
11-digit billing NDC 72407043040
UNII SOI2LOH54Z, 15FIX9V2JP, V06SV4M95S
Application # M020
SPL Set ID 4739179e-88b3-8820-e063-6394a90aa211
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-12-28
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; TITANIUM DIOXIDE; HOMOSALATE
Why two NDCs? The FDA registers this code as 72407-430-40 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 72407-0430-40. 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

LabelerPur-lisse Beauty, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code72407
First marketedDec 2022
Product typeHuman Otc Drug
Portfolio33 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?

Ageless Glow Serum BB Cream Sunscreen SPF 40 is a topical cream formulated as an over-the-counter monograph drug product. It contains three active ingredients that function as ultraviolet (UV) filters: homosalate, titanium dioxide, and zinc oxide. These mineral and chemical sunscreen agents are typically used together to help protect skin from UVA and UVB sun exposure when applied to the skin. This product is marketed under FDA's established rules for sunscreen category products rather than as an individually reviewed 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 TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII C5INA23HXF
    Arbutin is a natural compound found in plants that acts as a preservative in medicines. It helps prevent bacterial and fungal growth to keep the product stable and safe during storage.
  • UNII 6UQO3086C7
    A beneficial microorganism used as a probiotic ingredient to support digestive health and promote beneficial gut bacteria balance in the formulation.
  • UNII OT12HJU3AR
    A plant-derived compound used as a skin-conditioning agent and antioxidant in topical formulations. It helps stabilize the product and may improve skin feel and texture in creams or lotions.
  • 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 8YOY78GNNX
    A fragrant essential oil derived from ylang-ylang tree flowers. It's used as a flavoring and fragrance agent to improve the taste or scent of medicines.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • UNII 39W1PKE3JI
    Bergamot oil is a citrus extract from bergamot orange peel. It's used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • UNII AKN3KSD11B
    Orange oil obtained by cold pressing orange peel. It serves as a flavoring agent and fragrance in medicines to improve taste and aroma.
  • UNII 23NL8NQ187
    A plant extract from the cornelian cherry fruit, used as a natural colorant and flavoring agent in medicines. It may contribute mild taste and visual appeal to the formulation.
  • UNII D5RZ7MF1YF
    A plant extract from hawthorn fruit used as a natural coloring agent and flavoring ingredient. It may help give the medicine its color and taste while serving as a filler.
  • UNII 0J3G3O53ST
    Palmarosa oil is a fragrant plant-derived oil used as a flavoring agent and fragrance in medications. It helps mask unpleasant tastes or odors in oral medicines and improves overall product appeal.
  • UNII I445L28B12
    A silicone-based compound that acts as a lubricant and glidant in tablet and capsule formulations. It reduces friction between particles and on equipment surfaces, helping medicines flow smoothly during manufacturing and tablet compression.
  • UNII 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 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII VCA5491KVF
    A fragrant oil extracted from clove leaves, used as a flavoring and aromatic agent to mask unpleasant tastes or add pleasant scent to medicines.
  • UNII 7CTH8MD549
    A natural plant extract from gardenia fruit used as a colorant in medicines. It provides yellow to orange coloring and may help preserve product stability.
  • UNII WEF51750MT
    A synthetic oil derived from branched fatty acids, used as an emollient and lubricant in topical formulations to soften the skin and improve product spreadability and texture.
  • UNII 0Q8K841432
    A plant extract from jasmine flowers used as a fragrance and flavoring agent in medicines. It adds pleasant scent and taste to make the medication more appealing to take.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII TG711Q7A1Q
    A plant extract from Chinese wolfberry fruit, used as a natural coloring agent, flavor enhancer, or nutritional ingredient in some formulations.
  • UNII 8JC99XGU4W
    Soluble fish skin collagen is a protein derived from fish skin that acts as a binder and thickening agent in medicines. It helps hold ingredients together and gives the product the right texture or consistency.
  • UNII 8QDN200R1S
    A fragrant essential oil derived from white champaca flowers, used as a flavor and fragrance ingredient to make the medicine more pleasant-tasting or aromatic.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII 3K0J1S7QGC
    A fragrant essential oil derived from geranium flowers, used as a flavoring and fragrance agent to improve the taste and aroma of medicines.
  • 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 7Q0OK5DOT4
    A plant-derived emulsifier made from glycerin and ricinoleic acid (from castor oil). It helps blend oil and water-based ingredients together in formulations and improves product texture and stability.
  • UNII O4446S9CRA
    A synthetic oily liquid made from propylene glycol and fatty acids. It acts as a solvent and emulsifier to help dissolve or mix ingredients, and improves how the medicine spreads or absorbs in the body.
  • UNII ABS794681C
    A plant extract from schisandra berries used in traditional medicine. It may be included as a natural flavoring agent or for its potential antioxidant properties in the formulation.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII 01S2G2C1E4
    Sorbitan isostearate is an emulsifier derived from sorbitol and isostearic acid. It helps mix oil and water-based ingredients together and keeps them blended throughout the medicine's shelf life.
  • UNII 0W8RRI5W5A
    A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
  • UNII OLX698AH5P
    A clay mineral processed with a quaternary ammonium compound. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII 08MNR5YE2R
    A wax made in a laboratory to mimic natural beeswax. It's used as a coating, binder, and thickener to give medicines a smooth texture and protect them from moisture.
  • 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 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 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 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.

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

The official label also statesWater, Isotridecyl Isononanoate, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone,Propylene Glycol Dicaprylate/Dicaprate, Caprylic/Capric Triglyceride, Sorbitan Sesquioleate, Synthetic Beeswax, Arbutin, Sodium Chloride, Tribehenin, Polyglyceryl-3 Polyricinoleate, Stearalkonium Hectorite, Phenoxyethanol, Sorbitan Isostearate, Xanthan Gum, Ethylhexylglycerin, Triethoxycaprylylsilane, Adenosine, Olea Europaea (Olive) Fruit Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Lavandula Angustifolia (Lavender) Oil, Cananga Odorata Flower Oil, Citrus Aurantium Dulcis (Orange) Oil, Pelargonium Graveolens Flower Oil, Cymbopogon Martini Oil, Michelia Alba Flower Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Bakuchiol, Eucalyptus Globulus Leaf Oil, Tocopherol, Jasminum Officinale (Jasmine) Oil, 1,2-Hexanediol, Bacillus Ferment, Cornus Officinalis Fruit Extract, Crataegus Oxyacantha Fruit Extract, Lycium Chinense Fruit Extract, Gardenia Jasminoides Fruit Extract, Schisandra Chinensis Fruit Extract, Collagen Extract, Linalool, Limonene. May Contain: Iron Oxides (CI 77492, CI 77491, CI 77499)

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
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Deep 7 g/100mL; 5.09 g/100mL; 9.5 g/100mLthis 72407-0430-40 Pur-lisse 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

🏛️
2022
On the market since
Dec 2022
📍
2026
Currently FDA-listed
4 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
72407-0430-40 You're viewing this 1 TUBE in 1 CARTON (72407-430-40) / 40 mL in 1 TUBE 2022-12-28 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 ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 72407-430-40, 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: 72407-0430-40, written without dashes as 72407043040. 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 72407-0430-40, the first segment (72407) is the labeler code FDA assigned to Pur-lisse Beauty, LLC; the middle segment (0430) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (40) 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 Pur-lisse Beauty, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Pur-lisse Beauty, LLC 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 5 words ▾

Uses Use helps prevent sunburn.

⏱️ Dosage and Administration 96 words ▾

Directions For sunscreen use: Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating 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. to 2 p.m. Wear long-sleeve shirts, pants, hats and sunglasses Children under 6 months of age: Ask a doctor

⚠️ Warnings 54 words ▾

Warnings For external use only. Do not use on damage 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 Center right away.

🧪 Active Ingredient 10 words ▾

Active Ingredients Homosalate 9.5% Titanium Dioxide 5.09% Zinc Oxide 7.0%

🧪 Inactive Ingredients 124 words ▾

Inactive Ingredients Water, Isotridecyl Isononanoate, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone,Propylene Glycol Dicaprylate/Dicaprate, Caprylic/Capric Triglyceride, Sorbitan Sesquioleate, Synthetic Beeswax, Arbutin, Sodium Chloride, Tribehenin, Polyglyceryl-3 Polyricinoleate, Stearalkonium Hectorite, Phenoxyethanol, Sorbitan Isostearate, Xanthan Gum, Ethylhexylglycerin, Triethoxycaprylylsilane, Adenosine, Olea Europaea (Olive) Fruit Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Lavandula Angustifolia (Lavender) Oil, Cananga Odorata Flower Oil, Citrus Aurantium Dulcis (Orange) Oil, Pelargonium Graveolens Flower Oil, Cymbopogon Martini Oil, Michelia Alba Flower Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Bakuchiol, Eucalyptus Globulus Leaf Oil, Tocopherol, Jasminum Officinale (Jasmine) Oil, 1,2-Hexanediol, Bacillus Ferment, Cornus Officinalis Fruit Extract, Crataegus Oxyacantha Fruit Extract, Lycium Chinense Fruit Extract, Gardenia Jasminoides Fruit Extract, Schisandra Chinensis Fruit Extract, Collagen Extract, Linalool, Limonene.

May Contain: Iron Oxides (CI 77492, CI 77491, CI 77499)

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 72407-0429-40 · Pur-lisse 72407-0431-40 · Pur-lisse →
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.