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Eminence Bright Skin Moisturizer SPF 40 Sunscreen ZINC OXIDE 200 mg/mL Cream — NDC 15751-3503-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Eminence Bright Skin Moisturizer SPF 40 Sunscreen ZINC OXIDE 200 mg/mL Cream — NDC 15751-3503-2 (Billing 15751-3503-02)

by Eminence Organic Skin Care · 1 JAR in 1 BOX / 250 mL in 1 JAR

This is a package of Eminence Bright Skin Moisturizer SPF 40 Sunscreen ZINC OXIDE 200 mg/mL Cream from Eminence Organic Skin Care, marketed since Jan 2021 and currently FDA-listed.

NDC 15751-3503-02
🏷️ FDA NDC (as labeled) 15751-3503-2 billing pads the package segment with a zero
This package
Contains250 mL in 1 jar Pack sizes3 compare ↓
Product page 15751-3503-01 Also comes in: 60 mL 15751-3503-1 3 ml 15751-3503-3
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) 15751-3503-2
Product NDC 15751-3503
11-digit billing NDC 15751350302
UNII SOI2LOH54Z
UPC 0823638021366
Application # M020
SPL Set ID 4f2ba93d-ec19-40c1-b4ca-53898841f55b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-01
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 15751-3503-2 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 15751-3503-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is a topical cream moisturizer that contains zinc oxide as its active ingredient. Zinc oxide is commonly used in over-the-counter sunscreen products as a mineral UV filter that helps block ultraviolet radiation from the sun. This product is marketed as an OTC monograph drug, meaning it is sold under FDA's established rules for sunscreen products rather than as an individually approved application. The cream is applied to the skin to provide sun protection with a stated SPF of 40.

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 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.
Try another pack size: 60 mL 3 ml
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
15751-3503-01 15751-3503-1 Main listing 1 JAR in 1 BOX / 60 mL in 1 JAR 2021-01-01 — Active
15751-3503-02 You're viewing this 1 JAR in 1 BOX / 250 mL in 1 JAR 2021-01-01 — Active
15751-3503-03 15751-3503-3 3 mL in 1 PACKET 2021-01-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 jar in 1 box / 250 ml in 1 jar.
What NDC number is used to bill for this package of Eminence Bright Skin Moisturizer SPF 40 Sunscreen ZINC OXIDE 200 mg/mL Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lilikoi Mineral Defense Sport Sunscreen SPF 30 200 mg/mL 15751-3040-05 Eminence 1 tube — — FDA listed —
Eminence Tropical Vanilla Day Cream SPF 40 Sunscreen 200 mg/mL 15751-3500-01 Eminence 1 jar — — FDA listed —
Eminence Lilikoi Daily Defense Moisturizer SPF 40 Sunscreen 200 mg/mL 15751-3501-01 Eminence 1 jar — — FDA listed —
Eminence Bright Skin Moisturizer SPF 40 Sunscreen 200 mg/mLthis 15751-3503-02 Eminence 1 jar — — FDA listed —
Sport Broad Spectrum SPF50 Water Resistant 80 minutes Mineral Sunscreen UVA UVB Protection Stick 200 mg/mL 53675-0203-00 Aruba 30 ml — — FDA listed —
Broad Spectrum SPF50 Water Resistant (80 minutes) Mineral Sunscreen UVA UVB Protection Stick for Kids 200 mg/mL 53675-0205-00 Aruba 30 ml — — FDA listed —
THINKSPORT sunscreen SPF 50 200 mg/mL 60781-1001-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKSPORT Kids sunscreen SPF 50 200 mg/mL 60781-1002-03 thinkOperations,LLC 89 ml — — FDA listed —
THINKBABY Baby Sunscreen SPF 50 200 mg/mL 60781-1003-03 thinkOperations,LLC 89 ml — — FDA listed —
Think Every Day Face Sunscreen SPF 30 200 mg/mL 60781-1011-01 thinkOperations,LLC 59 ml — — FDA listed —
Think Aloe and Tea Leaves Zinc oxide 200 mg/mL 60781-4698-01 thinkOperations,LLC 89 ml — — FDA listed —
Raw Elements Daily Moisturizer Broad Spectrum SPF30 200 mg/mL 70680-0305-00 Raw 80 ml — — FDA listed —
SUNNY Q Broad Spectrum SPF-30 200 mg/mL 81738-0138-00 Sunny 100.55 ml — — FDA listed —
TIGER BABY Baby Sunscreen SPF-50 200 mg/mL 82247-0278-00 BRICKELL 5 ml — — FDA listed —
JOYSPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0354-00 JOYSPRING 30 ml — — FDA listed —
JOY SPRING Kids Mineral Sunscreen SPF-30 200 mg/mL 82552-0356-00 JOYSPRING 90 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 2w 200 mg/mL 76354-0471-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Super Shield Mineral Sunscreen SPF50 200 mg/mL 79265-7778-01 Babo 89 ml — — FDA listed —
GLC OG Natural Tinted SPF 30 Sunscreen 200 mg/mL 84747-0530-00 GUD 1 jar — — FDA listed —
Sun Bum 50 Mineral Sunscreen 1 OZ 200 mg/mL 69039-0797-01 Sun 30 ml — — FDA listed —
Everyday Coverage Tinted Sunscreen - Extra Light Tint 200 mg/mL 72592-0001-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 9w 200 mg/mL 76354-0474-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 14w 200 mg/mL 76354-0479-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 3N 200 mg/mL 76354-0480-01 e.l.f. 1 bottle — — FDA listed —
Dr. Mercola Broad Spectrum 200 mg/mL 71239-0787-23 Natural 236 ml — — FDA listed —
Vitamin C BB Beauty Balm Sheer Tint SFP 30 200 mg/mL 55560-0108-01 Andalou 1 tube — — FDA listed —
Everyday Coverage Tinted Sunscreen - Light Tint 200 mg/mL 72592-0002-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 12w 200 mg/mL 76354-0477-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 5N 200 mg/mL 76354-0481-01 e.l.f. 1 bottle — — FDA listed —
Derma E Vitamin C Weightless Moisturizer SPF 45 200 mg/mL 54108-0359-01 derma 1 bottle — — FDA listed —
Kypris Pot of Shade Heliotropic Broad Spectrum SPF 30 Sunscreen And Primer 200 mg/mL 70608-0001-01 Kypris 1 jar — — FDA listed —
Everyday Coverage Tinted Sunscreen - Medium Tint 200 mg/mL 72592-0003-60 MV 60 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 13w 200 mg/mL 76354-0478-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color plus Correct Sheer Beige SPF 30 200 mg/mL 55560-0110-01 Andalou 1 tube — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 1C 200 mg/mL 76354-0470-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 11w 200 mg/mL 76354-0476-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 8N 200 mg/mL 76354-0483-01 e.l.f. 1 bottle — — FDA listed —
Babo Botanicals Sensitive Baby Mineral Sunscreen SPF50 200 mg/mL 79265-8758-01 Babo 89 ml — — FDA listed —
Thinkbaby Clear Zinc SPF 30 200 mg/mL 60781-4175-03 thinkOperations,LLC 89 ml — — FDA listed —
Baby Bum Mineral 50 Sunscreen 200 mg/mL 69039-0686-00 Sun 88 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 4W 200 mg/mL 76354-0472-01 e.l.f. 1 bottle — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 7N 200 mg/mL 76354-0482-01 e.l.f. 1 bottle — — FDA listed —
Perfecting BB Beauty Balm Natural Tint SPF 30 200 mg/mL 55560-0104-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 200 mg/mL 69039-0728-01 Sun 88 ml — — FDA listed —
Vivaiodays Sunscreen with Turmeric 200 mg/mL 71778-0002-01 5SENCO 100 ml — — FDA listed —
Ultra Violette Future Screen Broad Spectrum SPF 50 200 mg/mL 84803-0103-15 Grace 15 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 10w 200 mg/mL 76354-0475-01 e.l.f. 1 bottle — — FDA listed —
1000 Roses CC Color Plus Correct Sheer Tan SPF 30 200 mg/mL 55560-0106-01 Andalou 1 tube — — FDA listed —
Sun Bum 50 Mineral Sunscreen 32 OZ 200 mg/mL 69039-0718-01 Sun 946 ml — — FDA listed —
Well People Bio Tint SPF 30 Sunscreen 6w 200 mg/mL 76354-0473-01 e.l.f. 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

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 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 2FXJ6SW4PK
    A plant extract from yarrow, used in some formulations as a natural flavoring agent or botanical ingredient to add taste or aroma to the medicine.
  • UNII 9M289NKI69
    Alchemilla xanthochlora flowering top is a plant-derived ingredient used as a traditional botanical additive. It may serve as a flavoring, coloring, or general botanical component in herbal formulations.
  • 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 3M5V3D1X36
    A plant extract from bearberry leaves, used in traditional medicine formulations. It may function as a natural flavoring agent or botanical additive in some preparations.
  • UNII QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII 6VNO72PFC1
    A natural oil extracted from avocado fruit. It's used in medicines as an emollient and carrier to help dissolve or deliver active ingredients and improve how the product feels on skin or mucous membranes.
  • 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 L56Z1JK48B
    A vegetable-derived ingredient used primarily as a natural colorant and flavoring agent in medicines. It provides orange-yellow color and mild taste to tablets, capsules, or liquids.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 00WNZ48OR9
    Chlorophyll is a green pigment found in plants. It's used in medicines as a colorant and may help mask unpleasant odors or tastes in the formulation.
  • 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 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 9SJI1LW39W
    A plant-derived ingredient from lemongrass, used as a fragrance or flavor component and possibly a preservative in medicines to improve taste or aroma.
  • 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 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII 2788Z9758H
    A plant extract from licorice root used as a sweetener, flavoring agent, and natural emulsifier in medicines. It helps improve taste and may aid in keeping ingredients evenly mixed throughout the product.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • 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 X1U1U0N90J
    A plant extract from common mallow flowers used in some formulations as a natural flavoring agent and to add color. It may also help soothe irritation in throat lozenges or similar products.
  • UNII 50D2ZE9219
    A plant extract from lemon balm leaves, used as a flavoring and aromatic ingredient to improve the taste and smell of the medicine.
  • UNII A389O33LX6
    A plant extract from peppermint leaves used as a flavoring agent to improve taste. It may also provide a cooling or soothing sensory effect in the medicine.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 88496G1ERL
    Sodium phytate is a plant-derived salt used in medications as a chelating agent and preservative. It helps stabilize formulations and may improve how the body absorbs certain minerals in the medicine.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII W6LFQ57E4M
    Primula veris is a plant extract from cowslip flowers. It's used in medicines as a flavoring agent and to add color or improve taste.
  • 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 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 O414PZ4LPZ
    A beta hydroxy acid derived from willow bark or synthesized chemically. In topical medicines, it acts as a keratolytic agent that helps soften and shed dead skin cells, improving penetration of active ingredients.
  • UNII 205MXS71H7
    A plant extract from white willow bark. It's used as a natural flavoring agent and may help preserve the medicine by providing mild antioxidant properties in the formulation.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 7ZBS06BH4B
    A synthetic surfactant derived from coconut or palm oil. It helps other ingredients blend evenly throughout the medicine and improves how the product spreads or dissolves, acting as an emulsifier and detergent.
  • UNII 469OTG57A2
    Sodium pyrrolidone carboxylate is a synthetic polymer derived from pyrrolidone chemistry. It functions as a solubilizer and binder in medications, helping dissolve poorly water-soluble drugs and hold tablet ingredients together.
  • UNII X045WJ989B
    Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
  • 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 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 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.

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

The official label also statesOrganic Phytonutrient Blend [Aloe Barbadensis (Aloe) Juice, Glycyrrhiza Glabra (Licorice) Root Extract*, Citrus Limon (Lemon) Peel Extract*, Cymbopogon Schoenanthus (Lemongrass) Extract*, Salix Alba (Willow) Bark Extract*, Arctostaphylos Uva Ursi (Bearberry) Leaf Extract*, Mentha Piperita (Peppermint) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract*, Salvia Officinalis (Sage) Extract*, and Vegetable Glycerin], Persea Gratissima (Avocado) Oil*, Hypoxis Rooperi (African Potato) Extract, Vegetable Glycerin*, Aloe Barbadensis (Aloe) Juice*, Butyrospermum Parkii (Shea Butter)*, Cetearyl Alcohol, Sodium Cetearyl Sulfate, Coco Caprylate/Caprate, Sempervivum Tectorum (Stone Crop) Extract*, Glyceryl Stearate, Malva Sylvestris (Mallow) Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract, Panthenol (Provitamin B5), Sodium Hyaluronate (Botanical Hyaluronic Acid), Hydrolyzed Caesalpinia Spinosa (Tara Tree) Gum, Com-Derived Methyl Glucose Sesquistearate, Soy Lecithin, Polyhydroxystaric Acid, Xanthan Gum, Lactic Acid, Ascorbyl Palmitate (Vitamin C Ester), Citrus Limon (Lemon) Oil, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, Chlorophyl, Sodium Benzoate, Potassium Sorbate, Sodium Phytate, Sodium PCA, Blocomplex2 (Euterpe Oleracea (Acai)*, Citrus Limon (Lemon)*, Malpighia Glabra (Barbados Cherry)*, Embica Officinalis (Indian Gooseberry)*, Adansonia Digitata (Baobab)*, Myrciaria Dubia (Camu Camu)*, Daucus Carota Sativa (Carrot)*, Cocos Nucifera (Coconut) Water*, Lycium Barbarum (Goji) Berry*, Tapioca Starch (from Cassava Root)*, Thioctic Acid (Alpha Lipoic Acid) and Ubiquinone (Coenzyme Q10)]. *Certified organic ingredient

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 marketedJan 2021
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 🧪 Active Ingredient 🧪 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 sun

⏱️ Dosage and Administration 93 words ▾

Directions 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 54 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 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 7 words ▾

Active Ingredients Zinc Oxide 20% Purpose Sunscreen

🧪 Inactive Ingredients 210 words ▾

Inactive Ingredients Organic Phytonutrient Blend [Aloe Barbadensis (Aloe) Juice, Glycyrrhiza Glabra (Licorice) Root Extract*, Citrus Limon (Lemon) Peel Extract*, Cymbopogon Schoenanthus (Lemongrass) Extract*, Salix Alba (Willow) Bark Extract*, Arctostaphylos Uva Ursi (Bearberry) Leaf Extract*, Mentha Piperita (Peppermint) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract*, Salvia Officinalis (Sage) Extract*, and Vegetable Glycerin], Persea Gratissima (Avocado) Oil*, Hypoxis Rooperi (African Potato) Extract, Vegetable Glycerin*, Aloe Barbadensis (Aloe) Juice*, Butyrospermum Parkii (Shea Butter)*, Cetearyl Alcohol, Sodium Cetearyl Sulfate, Coco Caprylate/Caprate, Sempervivum Tectorum (Stone Crop) Extract*, Glyceryl Stearate, Malva Sylvestris (Mallow) Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract, Panthenol (Provitamin B5), Sodium Hyaluronate (Botanical Hyaluronic Acid), Hydrolyzed Caesalpinia Spinosa (Tara Tree) Gum, Com-Derived Methyl Glucose Sesquistearate, Soy Lecithin, Polyhydroxystaric Acid, Xanthan Gum, Lactic Acid, Ascorbyl Palmitate (Vitamin C Ester), Citrus Limon (Lemon) Oil, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, Chlorophyl, Sodium Benzoate, Potassium Sorbate, Sodium Phytate, Sodium PCA, Blocomplex2 (Euterpe Oleracea (Acai)*, Citrus Limon (Lemon)*, Malpighia Glabra (Barbados Cherry)*, Embica Officinalis (Indian Gooseberry)*, Adansonia Digitata (Baobab)*, Myrciaria Dubia (Camu Camu)*, Daucus Carota Sativa (Carrot)*, Cocos Nucifera (Coconut) Water*, Lycium Barbarum (Goji) Berry*, Tapioca Starch (from Cassava Root)*, Thioctic Acid (Alpha Lipoic Acid) and Ubiquinone (Coenzyme Q10)]. *Certified organic ingredient

🎯 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 ↗

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 Eminence Bright Skin Moisturizer SPF 40 Sunscreen (this brand).

Top reported reactions

Macular Degeneration460
Pyrexia306
Nausea290
Pain282
Malaise261
Weight Decreased236
Therapeutic Product Effect Incomplete214

Reporter sex

1,941 reports
Male · 37%
Female · 63%
Unknown · 0%

Serious outcomes

Hospitalization988
Death204
Life-threatening116
Disabling32
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 272 82
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 jar (15751-3503-01), 3 ml (15751-3503-03). Each has its own NDC and its own page — see the package list near the top of this page.
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.
← 15751-3501-01 · Eminence 15751-3504-00 · 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.