Home › NDC Lookup › Ingredients › Zinc Oxide › 15751-3506-01
Eminence Radiant Protection SPF Fluid ZINC OXIDE 150 mg/mL Liquid — NDC 15751-3506-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Eminence Radiant Protection SPF Fluid ZINC OXIDE 150 mg/mL Liquid — NDC 15751-3506-1 (Billing 15751-3506-01)

by Eminence Organic Skin Care · 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE

This is a package of Eminence Radiant Protection SPF Fluid ZINC OXIDE 150 mg/mL Liquid from Eminence Organic Skin Care, marketed since Sep 2023 and currently FDA-listed. It is this product's only package size.

NDC 15751-3506-01
🏷️ FDA NDC (as labeled) 15751-3506-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

⚠️
Other active recalls for Zinc Oxide (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0212-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0206-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0202-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0207-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0209-2026
Class II · Oct 31, 2025 — cGMP deviations (Blossom Pharmaceuticals) · FDA recall D-0208-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 15751-3506-1
Product NDC 15751-3506
11-digit billing NDC 15751350601
UNII SOI2LOH54Z
Application # M020
SPL Set ID 002a4766-0c7e-4ec7-e063-6294a90a78d8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-09-01
Route TOPICAL
Dosage form LIQUID
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 15751-3506-1 — 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 → 15751-3506-01. 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.

Clinical

🧪 What is this product?

Eminence Radiant Protection SPF Fluid is a topical liquid sunscreen product sold as an over-the-counter monograph drug. The active ingredient is zinc oxide, a mineral UV filter that is commonly used in sunscreen formulations to help protect skin from ultraviolet (UV) radiation exposure. This product is applied directly to the skin as part of sun protection routines.

Supplement & herbal interactions

Some supplements/herbs that may interact with Zinc oxide (OTC drug) — tap one for details:

Dimethylsulfoxide (dmso)Moderate Turpentine OilModerate AlchemillaMinor
🌿 Every supplement checked against Zinc oxide (OTC drug) (3 interactions) — ranked by severity →
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.

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 mLPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
15751-3506-01 You're viewing this Main listing 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE 2023-09-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
SM SOLMIRAGE SUNCARE Solserum Mineral Sunscreen SPF 40 150 mg/mL 87018-0875-00 ALL 1 bottle — — FDA listed —
Fre Plump Me Peptide Lip Tint Pampelonne Spf 30 150 mg/mL 69435-1410-01 Peer 1 tube — — FDA listed —
Eminence Radiant Protection SPF Fluid 150 mg/mLthis 15751-3506-01 Eminence 1 bottle — — FDA listed —
Fre Plump Me Peptide Lip Tint Cassis Spf 30 150 mg/mL 69435-1411-01 Peer 1 tube — — FDA listed —
Hawaii Sol Natural Non-Nano Sunscreen SPF 50 150 mg/mL 82520-0957-00 Caribbean 177 ml — — FDA listed —
Caribbean Sol Natural Non-Nano Sunscreen SPF 50 150 mg/mL 82520-0956-00 Caribbean 177 ml — — FDA listed —
MIAMI BEACH BUM SPF-50 Blocked Sunscreen 150 mg/mL 82812-0448-00 MIAMI 177 ml — — FDA listed —
Fre Plump Me Peptide Lip Tint Monaco Spf 30 150 mg/mL 69435-1409-01 Peer 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
Sep 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.

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 46AM2VJ0AW
    A dried fruit powder from the acai berry, used as a natural colorant and flavor ingredient to add purple-red color and fruity taste to medicines and supplements.
  • UNII 51N9TR1W6P
    A natural plant extract from the baobab fruit, used as a thickener, emulsifier, and texture enhancer in medicines. It helps create a smooth consistency and may improve how the active ingredient disperses in the product.
  • 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 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII LED42LZG6O
    C13-16 isoparaffin is a mixture of refined mineral oils derived from petroleum. It acts as a solvent and emollient in topical formulations, helping dissolve active ingredients and soften the skin.
  • UNII U73D397055
    A blend of plant-derived fats and oils that act as a liquid carrier and solvent in medicines. It helps dissolve active ingredients and improve how the body absorbs them from capsules or liquid formulations.
  • UNII R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII 267F5Y81NT
    Coconut water is a natural liquid from inside coconut fruits. It's used in medicines as a vehicle or solvent to help dissolve and deliver active ingredients, and sometimes as a flavor or sweetening agent.
  • UNII F9I9HZH3O3
    A plant-derived ingredient from cultivated carrots. It may serve as a natural colorant, flavor component, or filler in the medication formulation.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • UNII WB5K9Y35Y9
    A synthetic crosslinked polymer made by combining hexamethylene diisocyanate with trimethylol hexyllactone. It's used as a film-former and binder to help create protective coatings on tablets or capsules and improve product stability.
  • UNII 39EYQ1W9RB
    A synthetic oil made from hydrogenated plant or petroleum waxes. It serves as a lubricant and glidant in tablet or capsule formulations to reduce friction during manufacturing and improve powder flow.
  • UNII 113171Q70B
    Lauroyl lysine is a compound made by combining an amino acid (lysine) with a fatty acid (lauric acid). It works as a glidant and lubricant to help powder particles flow smoothly during manufacturing and tablet compression.
  • UNII 24RS0A988O
    Lemon is a citrus fruit extract used as a natural flavoring agent and acidulant to add tart taste and help preserve medicines while improving their palatability.
  • UNII 930626MWDL
    A plant extract from goji berries used as a natural coloring agent and flavor enhancer in medicines. It may add color and taste while serving as a source of beneficial plant compounds in the formulation.
  • UNII B94O42LA9M
    A natural plant extract from the acerola cherry fruit, used as a source of vitamin C and as a colorant or flavor ingredient in medicines and supplements.
  • UNII FA9KFJ4Z6P
    A manufactured compound combining glucose (a natural sugar) with oleic acid (a fatty acid). It acts as an emulsifier and solubilizer, helping mix oil and water-based ingredients together in the medicine.
  • UNII YSW4EM1EKP
    A tropical fruit extract used as a natural color and flavor ingredient in medicines. It adds taste appeal and visual appearance to oral formulations.
  • 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 T9BY3B181Z
    A waxy substance derived from stearic acid (a fatty acid) combined with pentaerythritol. It serves as a lubricant and glidant in tablets and capsules, helping the medicine move smoothly through manufacturing equipment and preventing sticking during compression.
  • UNII YLX4CW2576
    A plant extract from the Indian gooseberry fruit, used as a natural source of vitamin C and antioxidants. It may function as a preservative or potency booster in formulations.
  • 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 R60QEP13IC
    Rice bran is a natural powder made from the outer layer of rice grains. It's used in medicines as a filler and flow agent to add bulk and help the product mix and flow smoothly during manufacturing.
  • UNII 24SC3U704I
    A powdery carbohydrate extracted from tapioca plant roots. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your digestive system.
  • UNII 73Y7P0K73Y
    Thioctic acid, also called alpha-lipoic acid, is an antioxidant compound. In medicines, it may be used as a stabilizer to protect other active ingredients from breaking down.
  • UNII 2P6O7CFW5K
    Triheptanoin is a synthetic fat made from glycerol and seven-carbon fatty acids. It's used as a caloric supplement and carrier in certain formulations to deliver active ingredients and provide nutritional support.
  • UNII EJ27X76M46
    Ubidecarenone is a naturally occurring compound found in cells that helps produce energy. In medicines, it acts as an antioxidant and may help stabilize the product while supporting cellular function in the body.

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

The official label also statesCaprylic/Capric Triglyceride*, Butyloctyl Salicylate, Oryza Sativa (Rice) Wax*, Copernicia Cerifera (Carnauba) Wax*, Triheptanoin, Pentaerythrityl Stearate/Caprate/Caprylate/Adipate, Polyhydroxystearic Acid, Lauroyl Lysine, Methyl Glucose Dioleate, Hydrogenated Poly(C6-20 Olefin),HDI/Trimethylol Hexyllactone Crosspolymer, Niacinamide (Vitamin B3), C13-16 Isoalkane, Bakuchiol, Natural Fragrance, Biocomplex2™ [Daucus Carota Sativa (Carrot) Seed Oil*, Euterpe Oleracea (Acai) Fruit Extract*, Citrus Limon (Lemon) Juice*, Malpighia Glabra (Barbados Cherry) Fruit Extract*, Emblica Officinalis (Indian Gooseberry) Fruit Extract*, Adansonia Digitata (Baobab) Fruit Extract*, Myrciaria Dubia (Camu Camu) Fruit Extract*, Daucus Carota Sativa (Carrot) Root Extract*, Cocos Nucifera (Coconut) Water*, Lycium Barbarum (Goji) Fruit Extract*, Helianthus Annuus (Sunflower) Seed Oil*, Plant-Derived Maltodextrin* and Vegetable Glycerin*].

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.

Manufacturer & labeler

LabelerEminence Organic Skin Care
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code15751
First marketedSep 2023
Product typeHuman Otc Drug
Portfolio14 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.

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 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 words ▾

Uses helps prevent sunburn 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

⏱️ Dosage and Administration 96 words ▾

Directions Shake well before 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. - 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses. Children under 6 months of age: Ask a doctor.

⚠️ Warnings 33 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 doctor if rash occurs

🧪 Inactive Ingredients 101 words ▾

Inactive Ingredients Caprylic/Capric Triglyceride*, Butyloctyl Salicylate, Oryza Sativa (Rice) Wax*, Copernicia Cerifera (Carnauba) Wax*, Triheptanoin, Pentaerythrityl Stearate/Caprate/Caprylate/Adipate, Polyhydroxystearic Acid, Lauroyl Lysine, Methyl Glucose Dioleate, Hydrogenated Poly(C6-20 Olefin),HDI/Trimethylol Hexyllactone Crosspolymer, Niacinamide (Vitamin B3), C13-16 Isoalkane, Bakuchiol, Natural Fragrance, Biocomplex2™ [Daucus Carota Sativa (Carrot) Seed Oil*, Euterpe Oleracea (Acai) Fruit Extract*, Citrus Limon (Lemon) Juice*, Malpighia Glabra (Barbados Cherry) Fruit Extract*, Emblica Officinalis (Indian Gooseberry) Fruit Extract*, Adansonia Digitata (Baobab) Fruit Extract*, Myrciaria Dubia (Camu Camu) Fruit Extract*, Daucus Carota Sativa (Carrot) Root Extract*, Cocos Nucifera (Coconut) Water*, Lycium Barbarum (Goji) Fruit Extract*, Helianthus Annuus (Sunflower) Seed Oil*, Plant-Derived Maltodextrin* and Vegetable Glycerin*].

🎯 Purpose 6 words ▾

Active Ingredient Purpose Zinc Oxide 15%............Sunscreen

📄 Keep Out of Reach of Children 19 words ▾

Keep out or reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel ~2 min read ▾

Radiant Protection SPF Fluid Drug Facts Active Ingredient Purpose Zinc Oxide 15%……………………...Sunscreen Uses helps prevent sunburn 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 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 Stop use and ask doctor if rash occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions Shake well before 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. – 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses. Children under 6 months of age: Ask a doctor. Other information Protect the product in this container from excessive heat and direct sun.

Inactive ingredients Caprylic/Capric Triglyceride*, Butyloctyl Salicylate, Oryza Sativa (Rice) Wax*, Copernicia Cerifera (Carnauba) Wax*, Triheptanoin, Pentaerythrityl Stearate/Caprate/Caprylate/Adipate, Polyhydroxystearic Acid, Lauroyl Lysine, Methyl Glucose Dioleate, Hydrogenated Poly(C6-20 Olefin), HDI/Trimethylol Hexyllactone Crosspolymer, Niacinamide (Vitamin B3), C13-16 Isoalkane, Bakuchiol, Natural Fragrance, Biocomplex2™ [Daucus Carota Sativa (Carrot) Seed Oil*, Euterpe Oleracea (Acai) Fruit Extract*, Citrus Limon (Lemon) Juice*, Malpighia Glabra (Barbados Cherry) Fruit Extract*, Emblica Officinalis (Indian Gooseberry) Fruit Extract*, Adansonia Digitata (Baobab) Fruit Extract*, Myrciaria Dubia (Camu Camu) Fruit Extract*, Daucus Carota Sativa (Carrot) Root Extract*, Cocos Nucifera (Coconut) Water*, Lycium Barbarum (Goji) Fruit Extract*, Helianthus Annuus (Sunflower) Seed Oil*, Plant-Derived Maltodextrin* and Vegetable Glycerin*].

DISTRIBUTED BY Éminence Organic Skin Care #300 - 530 West Broadway, Vancouver BC V5Z 1E9 www.eminenceorganics.com 1-888-747-6342 (US & Canada Toll Free) FORMULATED IN HUNGARY / Made in USA Refer to Radiant Protection SPF Fluid US 1.7oz Radiant Protection SPF Fluid US 1.7oz Box

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 — the ingredient across all brands.

Top reported reactions

Macular Degeneration460
Nausea365
Pyrexia351
Pain348
Malaise289
Weight Decreased284
Constipation257

Age at onset

Neonate6
Infant11
Child35
Adolescent8
Adult218
Elderly272

Reporter sex

0 reports
Male · 36%
Female · 64%
Unknown · 0%

Serious outcomes

Hospitalization1,368
Death290
Disabling63
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 365 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.

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Eminence Organic Skin Care. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Eminence Organic Skin Care 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.
← 15751-3504-00 · Eminence 15751-3508-01 · Eminence →
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.