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NUDESCREEN BLUSH TINT SPF 30 - SUNNY SWEET CHEEKS ZINC OXIDE SUNSCREEN 15 g/100mL Lotion — NDC 54111-0175-01 package photo

NUDESCREEN BLUSH TINT SPF 30 - SUNNY SWEET CHEEKS ZINC OXIDE SUNSCREEN 15 g/100mL Lotion

by Bentley Laboratories, LLC · 1 TUBE in 1 CARTON (54111-175-01) / 15 mL in 1 TUBE
NDC 54111-0175-01
🏷️ FDA NDC (as labeled) 54111-175-01 billing pads the product 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) 54111-175-01
Product NDC 54111-175
11-digit billing NDC 54111017501
UNII SOI2LOH54Z
Application # M020
SPL Set ID 5c98bacb-8bbd-47b8-8987-50be1ed34fc0
Established class (EPC) Copper Absorption Inhibitor
Physiologic effect Decreased Copper Ion Absorption
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-12-27
Route TOPICAL
Dosage form LOTION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 54111-175-01 — 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 → 54111-0175-01. 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

LabelerBentley Laboratories, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code54111
First marketedDec 2023
Product typeHuman Otc Drug
Portfolio35 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 an over-the-counter sunscreen lotion applied to the skin. Zinc oxide is a mineral UV filter that reflects and scatters ultraviolet light, and it is commonly used in sunscreen products to help protect skin from sun damage. The product is formulated as a tinted blush lotion with a sun protection factor of 30 and is marketed under FDA's monograph rules for sunscreen products.

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 9L3TIH1UUE
    Spirulina platensis is a blue-green algae used as a natural colorant and nutritional ingredient in supplements and some medications. It provides a blue-green color and may add protein and vitamins to the product.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • 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 CI87N1IM01
    A mixture of liquid hydrocarbons derived from petroleum, used as a lubricant and glidant to help the medicine flow smoothly during manufacturing and ensure even tablet coating or capsule filling.
  • UNII 8D9H4QU99H
    A synthetic fatty acid ester derived from coconut oil, used as an emulsifier and solubilizer to help mix oil and water-based ingredients and improve how the body absorbs certain drugs.
  • UNII 1E5KJY107T
    A liquid mixture derived from coconut oil, coconut alkanes serve as a solvent and lubricant in medicines. They help dissolve active ingredients and reduce friction during manufacturing and tablet compression.
  • UNII JFB4DJZ8BR
    A modified corn starch created by chemically linking starch molecules. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in the digestive system.
  • UNII 5B8915UELW
    A plant-derived compound used as an antioxidant in medicines. It helps prevent spoilage and degradation of active ingredients during storage by protecting them from oxidative damage.
  • 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII X33R8U0062
    Isostearic acid is a fatty acid derived from vegetable oils. It acts as an emulsifier and lubricant in medicines, helping blend ingredients together and reducing friction during tablet or capsule manufacturing.
  • UNII 2C1F12C6AP
    A beneficial live bacterium used as a probiotic ingredient. It's included to support the product's probiotic function by promoting beneficial microorganisms in the digestive system.
  • 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 7666FJ0J9F
    A rosin-derived compound used as a film-coating agent and binder in tablets and capsules. It helps create a protective layer around the medication and improves tablet hardness.
  • 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 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • UNII 602YE42W5R
    A natural extract from passion fruit that acts as a flavoring agent. It adds taste and aroma to make the medicine more palatable, particularly in liquid or chewable formulations.
  • UNII 687U3PEB2Y
    A complex emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients together and improves the texture and stability of creams, lotions, and other formulated products.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • 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 97K5YEF88C
    A clay-based ingredient used as a suspending agent and thickener in liquid medicines. It helps keep solid particles evenly distributed throughout the product so the medication mixes properly when shaken.
  • 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 06XEA2VD56
    Sorbitan oleate is an emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in the medicine.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 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 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 H92E6QA4FV
    Zinc stearate is a fine white powder made from zinc and stearic acid. It works as a lubricant and glidant to help the tablet or capsule move smoothly through manufacturing equipment and prevents sticking.

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

The official label also statesINACTIVE INGREDIENTS / INGRÉDIENTS INACTIFS: AQUA/WATER/EAU, COCONUT ALKANES, CAPRYLIC/CAPRIC TRIGLYCERIDE, PROPANEDIOL, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/ SEBACATE, COCO-CAPRYLATE/CAPRATE, METHYL DIHYDROABIETATE, SPIRULINA PLATENSIS EXTRACT, C15-19 ALKANE, SODIUM CHLORIDE, OCTYLDODECANOL, DISTARCH PHOSPHATE, ISOSTEARIC ACID, POLYHYDROXYSTEARIC ACID, IRON OXIDES (CI 77491), 1,2-HEXANEDIOL, BENZYL ALCOHOL, HYDROXYACETOPHENONE, ZINC STEARATE, QUATERNIUM-90 BENTONITE, ETHYL FERULATE, TRIETHYL CITRATE, BUTYLENE GLYCOL, MICA, IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), LACTOBACILLUS FERMENT, TITANIUM DIOXIDE (CI 77891), PASSIFLORA EDULIS FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, SORBITAN OLEATE

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
Nudescreen Blush Tint Spf 30- Sunset Rose 15 g/100mL 54111-0174-01 Bentley 1 tube — — FDA listed —
Nudescreen Blush Tint Spf 30 - Strawberry Sunburst 15 g/100mL 54111-0178-01 Bentley 1 tube — — FDA listed —
Nudescreen Blush Tint Spf 30 - Peaches N Sol 15 g/100mL 54111-0179-01 Bentley 1 tube — — FDA listed —
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow 15 g/100mL 54111-0194-01 Bentley 1 tube — — FDA listed —
Nudescreen Blush Tint Spf 30 - Sunny Sweet Cheeks 15 g/100mLthis 54111-0175-01 Bentley 1 tube — — FDA listed —
Nudescreen Blush Tint Spf 30 - Pink Sunrise 15 g/100mL 54111-0176-01 Bentley 1 tube — — FDA listed —
Nudescreen Blush Tint Spf 30 - Sunkissed 15 g/100mL 54111-0177-01 Bentley 1 tube — — FDA listed —
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Angel Glow 15 g/100mL 54111-0192-01 Bentley 1 tube — — FDA listed —
NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Goddess Glow 15 g/100mL 54111-0193-01 Bentley 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
Dec 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.

🔬 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 ZINC OXIDE SUNSCREEN — the ingredient across all brands.

Top reported reactions

Dry Skin1
Erythema1
Pruritus1
Skin Discomfort1
Skin Exfoliation1
Skin Fissures1
Skin Irritation1

Reporter sex

1 reports
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
54111-0175-01 You're viewing this 1 TUBE in 1 CARTON (54111-175-01) / 15 mL in 1 TUBE 2023-12-27 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 54111-175-01, 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: 54111-0175-01, written without dashes as 54111017501. 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 54111-0175-01, the first segment (54111) is the labeler code FDA assigned to Bentley Laboratories, LLC; the middle segment (0175) 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 Bentley Laboratories, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Bentley Laboratories, 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 120 words ▾

Uses / Usages • Sun Protection Factor 30 • Sunscreen • Helps prevent sunburn • Broad Spectrum (SPF 30) • UVA/UVB Protection • If used as directed with other sun protection measures [ see Directions ], decreases the risk of skin cancer and early skin aging caused by the sun. / • Facteur de protection solaire 30 • Crème solaire • Aide à prévenir les coups de soleil • F.P.S. 30 à Large spectre • Protection UVA/UVB • Si le produit est utilisé selon les instructions et avec d’autres mesures de protection contre le soleil [voir les Mode d’emploi] , le risque de cancer de la peau et de vieillissement prématuré de la peau causé par le soleil est réduit.

⏱️ Dosage and Administration ~1 min read ▾

Directions / Mode d’emploi • Adults and children over 6 months. • Apply generously and evenly 15 minutes before sun exposure. • Reapply at least every 2 hours/. • Adultes et enfants de plus de 6 mois • Appliquer abondamment/généreusement (et uniformément) 15 minutes avant l’exposition au soleil • Appliquer de nouveau au moins toutes les 2 heures • 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. / 11 a.m. – 3 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Test on a small area of skin before first use.

If irritation occurs (within 24 hours), use a different product • Use a water-resistant sunscreen if swimming or sweating • Children under 6 months of age: ask a doctor / Mesures de protection solaire: Passer du temps au soleil augmente le risque de cancer de la peau et du vieillissement prématuré de la peau. Afin de diminuer ce risque, il convient d’utiliser régulièrement un écran solaire avec un F.P.S. à large spectre d’au moins 15 et d’appliquer d’autres mesures de protection contre le soleil, telles que: limiter le temps passé au soleil, notamment entre 10h - 14h / 11h - 15h • Porter des chemises à manches longues, des pantalons, un chapeau et des lunettes de soleil. • Avant d’utiliser, appliquer sur une petite surface de la peau.

Si une irritation se produit (dans un délai de 24 heures), utiliser une autre produit que celui-ci. • Utiliser un écran solaire résistant à l’eau lors d’une activité aquatique ou s’il y a transpiration. • Enfants de moins de 6 mois: consulter un médecin

⚠️ Warnings 75 words ▾

Warnings / Mises en garde For external use only / Pour usage externe seulement When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. / Lorsque vous utilisez ce produit é viter tout contact avec les yeux. Le cas échéant, bien rincer avec de l’eau. Stop use and consult a health care practitioner if rash occurs. / Arrêter l’utilisation et consultez un professionnel de la santé en cas d’éruption cutanée

🧪 Active Ingredient 19 words ▾

Drug Facts / Info-Médicament ACTIVE INGREDIENTS (W/W) / INGRÉDIENTS ACTIFS (P/P): ZINC OXIDE 15% / OXYDE DE ZINC 15%

🧪 Inactive Ingredients 74 words ▾

INACTIVE INGREDIENTS / INGRÉDIENTS INACTIFS: AQUA/WATER/EAU, COCONUT ALKANES, CAPRYLIC/CAPRIC TRIGLYCERIDE, PROPANEDIOL, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/ SEBACATE, COCO-CAPRYLATE/CAPRATE, METHYL DIHYDROABIETATE, SPIRULINA PLATENSIS EXTRACT, C15-19 ALKANE, SODIUM CHLORIDE, OCTYLDODECANOL, DISTARCH PHOSPHATE, ISOSTEARIC ACID, POLYHYDROXYSTEARIC ACID, IRON OXIDES (CI 77491), 1,2-HEXANEDIOL, BENZYL ALCOHOL, HYDROXYACETOPHENONE, ZINC STEARATE, QUATERNIUM-90 BENTONITE, ETHYL FERULATE, TRIETHYL CITRATE, BUTYLENE GLYCOL, MICA, IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), LACTOBACILLUS FERMENT, TITANIUM DIOXIDE (CI 77891), PASSIFLORA EDULIS FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, SORBITAN OLEATE

🎯 Purpose 5 words ▾

Purpose / Utilite Sun Protectant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 54111-0174-01 · Bentley 54111-0176-01 · Bentley →
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.