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Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light ZINC OXIDE 67 mg/mL Emulsion — NDC 84003-0051-01 package photo

Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light ZINC OXIDE 67 mg/mL Emulsion

by Dolce & Gabbana Beauty S.R.L · 1 BOTTLE in 1 BOX (84003-051-01) / 30 mL in 1 BOTTLE
NDC 84003-0051-01
🏷️ FDA NDC (as labeled) 84003-051-01 billing pads the product segment with a zero
This package
Contains30 mL in 1 bottle Pack sizes2 compare ↓
Also comes in: 30 mL 84003-0051-02
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

⚠️
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

FDA NDC (as labeled) 84003-051-01
Product NDC 84003-051
11-digit billing NDC 84003005101
UNII SOI2LOH54Z
UPC 8054754408973, 8054754408669
Application # M
SPL Set ID d2930d0e-c622-4843-87f2-fa1a92837ff2
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-01-01
Route TOPICAL
Dosage form EMULSION
Substance ZINC OXIDE
Why two NDCs? The FDA registers this code as 84003-051-01 — 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 → 84003-0051-01. 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

LabelerDolce & Gabbana Beauty S.R.L
FDA applicationM (OTC MONOGRAPH DRUG)
Labeler code84003
First marketedJan 2025
Product typeHuman Otc Drug
Portfolio59 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 a tinted emulsion (liquid) applied to the skin that contains zinc oxide, an inorganic UV filter commonly used in sunscreen products. Zinc oxide reflects and scatters ultraviolet radiation to help protect skin from sun exposure. This product is marketed as an OTC monograph drug, meaning it is formulated and labeled according to FDA's established guidelines for over-the-counter sunscreen ingredients rather than as an individually approved drug 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.

🧪 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 KD6TZ2QICH
    A synthetic humectant and skin-conditioning agent derived from menthol. It's used in topical formulations to help retain moisture, improve texture, and enhance the feel of the product on skin.
  • 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 5QB0T2IUN0
    Aluminum hydroxide is a white powder mineral compound used as an antacid ingredient in some formulations. It works as a buffer and pH regulator to help neutralize stomach acid in the medicine.
  • UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII 9P2U39H18W
    Bilberry is a natural plant extract from bilberry fruit. It's used in medicines as a colorant and flavoring agent to improve taste and appearance.
  • UNII X2I70H0QJE
    A silicone-based polymer made from polyethylene glycol and polypropylene glycol chains. It works as an emulsifier and surfactant, helping mix water and oil ingredients together and improving the texture and spreadability of creams, lotions, and other topical products.
  • UNII 2KAG279R6R
    Dehydroacetic acid is a synthetic preservative that prevents mold, yeast, and bacterial growth in medicines. It extends shelf life by protecting the product from spoilage during storage and use.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 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 3297VXM8Z6
    A plant-derived humectant and emollient made from glycerin and glucose. It helps retain moisture in the formulation and improves texture and spreadability in topical products.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII 411THY156Q
    Isostearyl neopentanoate is a synthetic oily substance used as an emollient and skin-conditioning agent in topical medicines. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • 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 6HQ855798J
    Laureth-4 is a synthetic detergent made from lauryl alcohol and ethylene oxide. It acts as an emulsifier and solubilizer, helping blend oil and water-based ingredients and improve how the body absorbs the active drug.
  • UNII DE08037SAB
    Magnesium sulfate is a mineral salt that acts as an osmotic agent in medications. It draws water into the intestines to soften stool or is used as a filler and processing aid in some solid dosage forms.
  • 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 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII DR0K5NOJ4R
    Phenyl trimethicone is a silicone-based lubricant and glidant. It helps powder particles flow smoothly and reduces friction during tablet or capsule manufacturing and filling.
  • 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 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • 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 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 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 8W46YN971G
    Sodium dehydroacetate is a salt derived from dehydroacetic acid, a compound used as a preservative. It helps prevent mold, bacteria, and yeast growth in medicines, extending shelf life and maintaining product safety.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesWATER/EAU (AQUA), DIMETHICONE, C12-15 ALKYL BENZOATE, PHENYL TRIMETHICONE, TALC, PEG-10 DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TRIMETHYLSILOXYSILICATE, GLYCERIN, ISOSTEARYL NEOPENTANOATE, GLYCERYL GLUCOSIDE, BIS-PEG/PPG-14/14 DIMETHICONE, ISODODECANE, PHENOXYETHANOL, SODIUM CHLORIDE, MICA, MAGNESIUM SULFATE, MENTHOXYPROPANEDIOL, SODIUM DEHYDROACERARE, HYDROGEN DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, BENZOIC ACID, C24-28 ALKYL METHICONE, DISTEARDIMONIUM HECTORITE, SILICA, ALUMINUM HYDROXIDE, DEHYDROACETIC ACID, VACCINIUM MYRTILLUS FRUIT EXTRACT, PROPYLENE CARBONATE, ETHYLHEXYLGLYCERIN, LAURETH-4, POTASSIUM SORBATE, SODIUM BENZOATE, LACTIC ACID, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE: +/- MAY CONTAIN: TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499)

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer 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.
Try another pack size: 30 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dolce and Gabbana Blueberry Nutri Tint SPF 20 2C Light 67 mg/mL 84003-0048-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 18N Medium 67 mg/mL 84003-0060-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 22N Medium 67 mg/mL 84003-0063-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 28W Medium Deep 67 mg/mL 84003-0067-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 29W Medium Deep 67 mg/mL 84003-0068-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 35W Deep 67 mg/mL 84003-0072-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 37W Deep 67 mg/mL 84003-0074-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 19W Medium 67 mg/mL 84003-0061-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 1N Light 67 mg/mL 84003-0047-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 11W Light Medium 67 mg/mL 84003-0055-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 31N Medium Deep 67 mg/mL 84003-0070-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 36N Deep 67 mg/mL 84003-0073-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 3W Light 67 mg/mL 84003-0049-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 5N Light 67 mg/mL 84003-0050-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light 67 mg/mLthis 84003-0051-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 12N Light Medium 67 mg/mL 84003-0056-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 17W Medium 67 mg/mL 84003-0059-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 15N Light Medium 67 mg/mL 84003-0057-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 16N Light Medium 67 mg/mL 84003-0058-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 24N Medium 67 mg/mL 84003-0064-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 26C Medium Deep 67 mg/mL 84003-0066-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 34W Deep 67 mg/mL 84003-0071-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 10N Light Medium 67 mg/mL 84003-0054-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 30N Medium Deep 67 mg/mL 84003-0069-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 21W Medium 67 mg/mL 84003-0062-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 40C Deep 67 mg/mL 84003-0076-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 9C Light Medium 67 mg/mL 84003-0053-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 39N Deep 67 mg/mL 84003-0075-01 DOLCE 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 7N Light 67 mg/mL 84003-0052-01 Dolce 1 bottle — — FDA listed —
Dolce and Gabbana Blueberry Nutri Tint SPF 20 25W Medium Deep 67 mg/mL 84003-0065-01 DOLCE 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

🏛️
2025
On the market since
Jan 2025
📍
2026
Currently FDA-listed
1 year 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 Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light (this brand).

Top reported reactions

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

Age at onset

Neonate5
Infant8
Child28
Adolescent5
Adult110
Elderly192

Reporter sex

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

Serious outcomes

Hospitalization988
Life-threatening116
Disabling32
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 272 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
84003-0051-01 You're viewing this 1 BOTTLE in 1 BOX (84003-051-01) / 30 mL in 1 BOTTLE 2025-01-01 Active
84003-0051-02 1 BOTTLE in 1 BOX (84003-051-02) / 30 mL in 1 BOTTLE 2025-01-01 Active

Pack size FAQ

What quantity is in NDC 84003-0051-01?
NDC 84003-0051-01 is listed by the FDA — 1 bottle in 1 box / 30 ml in 1 bottle.
What NDC number is used to bill for this package of Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light ZINC OXIDE 67 mg/mL Emulsion?
Bill NDC 84003-0051-01 — the 11-digit billing format is 84003005101. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 84003-051-01, 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: 84003-0051-01, written without dashes as 84003005101. 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 84003-0051-01, the first segment (84003) is the labeler code FDA assigned to Dolce & Gabbana Beauty S.R.L; the middle segment (0051) 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 Dolce & Gabbana Beauty S.R.L. 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 1 other package presentation of this same product, including 1 bottle (84003-0051-02). 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?
Dolce & Gabbana Beauty S.R.L 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 29 words ▾

Uses Helps prevent sunburn If uses directed with others sun protection measures (see Directions ) decreases the risk of skin cancer and early skin aging caused by the sun.

⏱️ Dosage and Administration 95 words ▾

Directions Apply generously 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 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 SHAKE WELL BEFORE USE

⚠️ 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 6.7% Purpose Sunscreen

🧪 Inactive Ingredients 85 words ▾

Inactive ingredients WATER/EAU (AQUA), DIMETHICONE, C12-15 ALKYL BENZOATE, PHENYL TRIMETHICONE, TALC, PEG-10 DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TRIMETHYLSILOXYSILICATE, GLYCERIN, ISOSTEARYL NEOPENTANOATE, GLYCERYL GLUCOSIDE, BIS-PEG/PPG-14/14 DIMETHICONE, ISODODECANE, PHENOXYETHANOL, SODIUM CHLORIDE, MICA, MAGNESIUM SULFATE, MENTHOXYPROPANEDIOL, SODIUM DEHYDROACERARE, HYDROGEN DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, BENZOIC ACID, C24-28 ALKYL METHICONE, DISTEARDIMONIUM HECTORITE, SILICA, ALUMINUM HYDROXIDE, DEHYDROACETIC ACID, VACCINIUM MYRTILLUS FRUIT EXTRACT, PROPYLENE CARBONATE, ETHYLHEXYLGLYCERIN, LAURETH-4, POTASSIUM SORBATE, SODIUM BENZOATE, LACTIC ACID, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE: +/- MAY CONTAIN: TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499)

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84003-0050-01 · Dolce 84003-0052-01 · Dolce →
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.