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Eminence Daily Defense Tinted SPF ZINC OXIDE 115 mg/mL Liquid — NDC 15751-3508-1 (Billing 15751-3508-01)

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

This is a package of Eminence Daily Defense Tinted SPF ZINC OXIDE 115 mg/mL Liquid from Eminence Organic Skin Care, marketed since Jun 2024 and currently FDA-listed. It is this product's only package size.

NDC 15751-3508-01
🏷️ FDA NDC (as labeled) 15751-3508-1 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) 15751-3508-1
Product NDC 15751-3508
11-digit billing NDC 15751350801
UNII SOI2LOH54Z
Application # M020
SPL Set ID 14854bad-317e-154d-e063-6294a90a884f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-06-01
Route TOPICAL
Dosage form LIQUID
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 15751-3508-1 — 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 → 15751-3508-01. 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 Daily Defense Tinted SPF is a topical liquid sunscreen product marketed under the FDA's over-the-counter monograph rules for sunscreens. It contains zinc oxide, a mineral UV filter that is commonly used in sunscreen formulations to help protect skin from ultraviolet radiation. The tinted liquid form is applied to the skin and functions as a physical sunscreen barrier. This product is regulated as an OTC monograph drug rather than through individual FDA application.

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
15751-3508-01 You're viewing this Main listing 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE 2024-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Eminence Daily Defense Tinted SPF 115 mg/mLthis 15751-3508-01 Eminence 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2024
On the market since
Jun 2024
📍
2026
Currently FDA-listed
2 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 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 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 A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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 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 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 055456JHI7
    A natural substance derived from bitter orange peel. It's used as a flavoring agent and fragrance to improve the taste and smell of the medication.
  • UNII 0HNC1J1YED
    A natural oil extracted from lemon fruit, used as a flavoring agent to mask bitter tastes and add pleasant citrus flavor to medicines. It also helps improve the overall taste of the product.
  • UNII 6A7N43E0OJ
    A natural oil from grapefruit peel used as a flavoring agent to improve taste and provide a citrus scent to the medicine.
  • 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 OI7E2Z4LTA
    A natural oil extracted from carrot roots. It's used as a flavoring agent and fragrance component to add taste and aroma to the medicine.
  • UNII Y57H6218HP
    A plant-derived ingredient from the South American açaí berry. It's used as a natural colorant, flavor component, and antioxidant in formulations.
  • 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 C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • UNII SAS9Z1SVUK
    A natural oil extracted from ginger root that adds flavor and aroma to the medicine. It may also serve as a preservative or help mask unpleasant tastes in the formulation.
  • 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 17S27ZT6KR
    A plant extract from sunflower seeds used as a natural emulsifier and skin-conditioning agent in topical formulations. It helps blend oil and water components together and softens the product texture.
  • UNII BU2OC48XBR
    Heptyl glucoside is a plant-derived surfactant, a substance that helps mix oil and water-based ingredients. It's used in medicines as an emulsifier and solubilizer to create uniform, stable formulations.
  • UNII H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • 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 9YT4B71U8P
    A plant extract from lavender flowers used as a flavoring and fragrance agent in medicines. It adds taste or aroma to improve how the product smells and tastes.
  • UNII 834K0WOS5G
    A natural fat extracted from sunflower seeds. It acts as an emulsifier and lubricant in medicines, helping mix ingredients that don't normally blend together and allowing the product to flow smoothly during manufacturing.
  • UNII AGN709ANTJ
    A natural liquid extracted from lemons, containing citric acid and water. It's used as a flavoring agent and acidifying ingredient to enhance taste and help maintain the medicine's pH balance.
  • 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 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • 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 1XGW49AK2J
    A natural oil derived from prickly pear cactus seeds. It's used in medicines as an emollient to soften and smooth the product's texture, and sometimes as a skin-conditioning agent in topical formulations.
  • 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 0F897O3O4M
    A naturally occurring alcohol derived from plants or synthesized chemically. It functions as a preservative and flavoring agent in medicines, helping prevent microbial growth and add pleasant taste to oral products.
  • 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 9229XJ4V12
    A synthetic emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients in formulations, keeping them mixed and preventing separation.
  • UNII 46P231IQV8
    A synthetic emulsifier derived from glycerin and fatty acids. It helps blend oil and water-based ingredients together in cosmetic and pharmaceutical formulations to create stable, uniform products.
  • UNII MZQ63P0N0W
    A plant-derived emulsifier made from glycerin and castor oil. It helps mix oil and water ingredients together in formulations like creams and lotions, keeping them blended.
  • 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 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 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 IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • UNII 65UEH262IS
    Safflower oil is a plant-based oil extracted from safflower seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and sometimes as an emollient to improve texture.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII D24K2Q1F6H
    A plant oil extracted from jojoba seeds. It acts as an emollient and conditioning agent in topical formulations, helping soften skin and improve product texture and spreadability.
  • 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 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • 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 R9N3379M4Z
    Sunflower seed is a plant-derived ingredient used as a filler and source of oil in medications. It helps add bulk to the formulation and may serve as a natural binding or lubricating component.
  • UNII 5EHL50I4MY
    A sodium salt compound used as a chelating agent in medicines. It binds to metals and minerals to improve stability, prevent discoloration, and help the medication stay effective longer.
  • 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 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 AZQ08K38Z1
    A synthetic oily liquid derived from salicylic acid. It works as an emollient and penetration enhancer in topical formulations, helping active ingredients absorb into skin while conditioning and softening the application area.
  • UNII 7L6DL16P1T
    Tropolone is a naturally occurring organic compound used in medicines as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the product.
  • 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.
  • UNII 0A3F415158
    A flavoring extract from vanilla bean fruit that gives medicine a pleasant vanilla taste and aroma. It masks bitter or unpleasant flavors to make the medicine easier to take.

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

The official label also statesAloe Barbadensis (Aloe) Leaf Juice*, Caprylic/Capric Triglyceride*, Tridecyl Salicylate, Vegetable Glycerin, Simmondsia Chinensis (Jojoba) Seed Oil*, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Methylpropanediol, Silica, Polyglyceryl-2 Dipolyhydroxystearate, Opuntia Ficus-Indica (Prickly Pear) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Oryza Sativa (Rice) Bran Extract, Citrus Limon (Lemon) Fruit Extract, Zingiber Officinale (Ginger) Root Extract, Citrus Aurantium Dulcis (Orange) Peel Extract, Sodium Hydroxide, Tocopherol (Vitamin E), Zingiber Officinale (Ginger) Root Oil, Salvia Officinalis (Sage) Leaf Extract, Hydrogenated Plant-Derived Lecithin, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Pelargonium Graveolens (Geranium) Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Vanilla Planifolia (Vanilla) Fruit Extract, Carthamus Tinctorius (Safflower) Seed Oil, Sodium Chloride, Iron Oxides, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Polyricinoleate, C12-15 Alkyl Benzoate, Plant-Derived Lecithin, Stearalkonium Hectorite, Caprylyl Glycol, Phenylpropanol, Helianthus Annuus (Sunflower) Extract, Tetrasodium Glutamate Diacetate, Vegetable Heptyl Glucoside, Corn-Derived Propanediol, 1,2-Hexanediol, Caprylyl Glycol, Tropolone, Biocomplex2™ [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*, Vegetable Glycerin*, Thioctic Acid (Alpha Lipoic Acid) and Ubiquinone (Coenzyme Q10)].

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 marketedJun 2024
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
🎯 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 34 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 Stop use and ask doctor if rash occurs

🧪 Inactive Ingredients 209 words ▾

Inactive Ingredients Aloe Barbadensis (Aloe) Leaf Juice*, Caprylic/Capric Triglyceride*, Tridecyl Salicylate, Vegetable Glycerin, Simmondsia Chinensis (Jojoba) Seed Oil*, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Methylpropanediol, Silica, Polyglyceryl-2 Dipolyhydroxystearate, Opuntia Ficus-Indica (Prickly Pear) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Oryza Sativa (Rice) Bran Extract, Citrus Limon (Lemon) Fruit Extract, Zingiber Officinale (Ginger) Root Extract, Citrus Aurantium Dulcis (Orange) Peel Extract, Sodium Hydroxide, Tocopherol (Vitamin E), Zingiber Officinale (Ginger) Root Oil, Salvia Officinalis (Sage) Leaf Extract, Hydrogenated Plant-Derived Lecithin, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Pelargonium Graveolens (Geranium) Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Vanilla Planifolia (Vanilla) Fruit Extract, Carthamus Tinctorius (Safflower) Seed Oil, Sodium Chloride, Iron Oxides, Polyglyceryl-3 Diisostearate, Polyglyceryl-3 Polyricinoleate, C12-15 Alkyl Benzoate, Plant-Derived Lecithin, Stearalkonium Hectorite, Caprylyl Glycol, Phenylpropanol, Helianthus Annuus (Sunflower) Extract, Tetrasodium Glutamate Diacetate, Vegetable Heptyl Glucoside, Corn-Derived Propanediol, 1,2-Hexanediol, Caprylyl Glycol, Tropolone, Biocomplex2™ [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*, Vegetable Glycerin*, Thioctic Acid (Alpha Lipoic Acid) and Ubiquinone (Coenzyme Q10)].

🎯 Purpose 6 words ▾

Active Ingredient Purpose Zinc Oxide 11.5%……………………...Sunscreen

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

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 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.
← 15751-3506-01 · Eminence 15751-3600-02 · 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.