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NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 ZINC OXIDE 18.4 g/100mL; 2 g/100mL Cream — NDC 71447-0033-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 ZINC OXIDE 18.4 g/100mL; 2 g/100mL Cream — NDC 71447-033-01 (Billing 71447-0033-01)

by LABORATOIRES DRUIDE INC · 1 TUBE in 1 BOX / 30 mL in 1 TUBE

This is a package of NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 ZINC OXIDE 18.4 g/100mL; 2 g/100mL Cream from LABORATOIRES DRUIDE INC, marketed since May 2024 and currently FDA-listed. It is this product's only package size.

NDC 71447-0033-01
🏷️ FDA NDC (as labeled) 71447-033-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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

NDC database record

One package, one record: these facts belong to NDC 71447-033-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71447 labeler · 033 product · 01 package
Package marketed since
May 27, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0829852146311
FDA record last changed
Aug 27, 2026
⚠️
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) 71447-033-01
Product NDC 71447-033
11-digit billing NDC 71447003301
UNII SOI2LOH54Z, 15FIX9V2JP
UPC 0829852146311
Application # M020
SPL Set ID 19af4441-31b2-72db-e063-6394a90a813c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-27
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; TITANIUM DIOXIDE
Why two NDCs? The FDA registers this code as 71447-033-01 — 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 → 71447-0033-01. 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?

This is a tinted sunscreen cream containing titanium dioxide and zinc oxide, which are mineral UV filters commonly used in sun-protection products. Applied topically to the skin, these ingredients function to reflect and scatter ultraviolet radiation from the sun. The product is marketed as an over-the-counter monograph drug, meaning it follows the FDA's established safety and use rules for sunscreen products rather than being individually reviewed. The formulation also provides light tinting and is labeled SPF 30.

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.
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
71447-0033-01 You're viewing this Main listing 1 TUBE in 1 BOX / 30 mL in 1 TUBE 2024-05-27 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Nelly Devuyst Biosolar Colorlift 3 Tinted Sunscreen Spf30 18.4 g/100mL; 2 g/100mLthis 71447-0033-01 LABORATOIRES 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2024
On the market since
May 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 S95658MI3W
    A carbohydrate derived from starch that acts as a binder and filler in tablets and capsules. It helps hold ingredients together and adds bulk to the medicine so it's easier to manufacture and handle.
  • UNII 1O11RD9U53
    A plant extract from acmella oleracea flowers. It acts as a flavoring agent and may provide a mild sensory effect to the medicine's taste or mouth-feel.
  • UNII E0M52HIR1Y
    A plant-derived oil extracted from horse chestnut seeds. It acts as an emollient and skin-conditioning agent in topical formulations, helping to soften and protect the product's texture.
  • 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 LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII B423VGH5S9
    A natural fruit ingredient derived from apples, used as a flavoring agent and sweetener to improve taste and palatability of the medicine.
  • UNII 2V52R0NHXW
    Ascorbyl glucoside is a stable form of vitamin C derived from ascorbic acid and glucose. It functions as an antioxidant in medicines to protect other ingredients from breaking down when exposed to air or light.
  • 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 43AGM4PHPI
    A mixture of plant or animal oils and fats with 10 to 18 carbon chains. Used as a solvent and carrier to dissolve or suspend active ingredients, helping deliver the medicine effectively.
  • UNII 9I2BJY2J17
    A plant extract from tea flowers used as a natural coloring agent and antioxidant in medicines. It helps maintain product stability and may provide a subtle color to the formulation.
  • UNII 76GTF6Z97M
    A natural fragrance extract from the tropical cananga tree flower. Used as a flavoring and scent agent to improve the taste and aroma of medicines.
  • UNII 6W864D0X3X
    A fragrant plant oil from cananga tree leaves, used as a flavoring and fragrance agent to improve the taste and aroma of the medicine.
  • UNII 8QF5D5H6UH
    A flavoring agent derived from cantaloupe fruit, used to add taste and aroma to medicines. It helps mask bitter or unpleasant flavors in oral formulations.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII 4UD6VQR2UP
    A natural extract from cinnamon twigs used as a flavoring agent and aromatic ingredient to improve the taste and smell of medications.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII K48IKT5321
    A plant extract from clove buds used as a flavoring agent and natural fragrance in medications. It adds taste and aroma to improve how the medicine smells and tastes.
  • 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 HOX6BEK27Q
    A natural extract from coffee fruit used as a flavoring agent to add taste to the medicine. It helps mask unpleasant flavors and improve how the product tastes.
  • UNII 6D5V13045W
    A plant extract from European beech flower buds used in some herbal or botanical formulations. It may serve as an active botanical ingredient or flavoring agent depending on the product's intended use.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII OU4GI2R2WB
    A blend of fragrance compounds that adds a fresh citrus and floral scent to the medicine. Fragrances mask unpleasant tastes or odors to make the product more pleasant to use.
  • UNII 6YSS42VSEV
    Fructose is a natural sugar derived from fruits and plants. It's used in medicines as a sweetener and filler to improve taste and add bulk to tablets or syrups.
  • 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 309GSC92U1
    Glycogen is a carbohydrate derived from animal sources that acts as a binder and filler in tablets and capsules. It helps hold ingredients together and adds bulk to the medicine's solid form.
  • 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 6OG06384ID
    A plant extract from jasmine leaves used as a flavoring agent and fragrance ingredient to improve the taste and aroma of medicines.
  • UNII 7F0EV20QYL
    Jojoba oil is a liquid wax extracted from jojoba plant seeds. In medications, it serves as an emollient and carrier oil that helps soften skin, improve texture, and distribute active ingredients evenly in topical formulations.
  • UNII L4J6XXD1E0
    Kigelia africana fruit extract is a natural plant-derived ingredient used as a flavoring agent or botanical additive in some formulations. It may contribute taste or plant-based properties to the medicine.
  • UNII I9GRO824LL
    Lemon oil is a natural fragrant extract from lemon peel. It's used in medicines as a flavoring agent to mask unpleasant tastes and improve how the medicine tastes to patients.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • UNII 6H1JQK35LA
    A dried flower extract from the early purple orchid plant, used as a traditional botanical ingredient. It may function as a binder or natural flavoring agent in herbal formulations.
  • UNII 4A0NCJ6RD6
    Polyglycerin-3 is a synthetic ingredient made by linking multiple glycerin molecules together. It acts as an emulsifier and humectant, helping oils and water mix smoothly and keeping the product from drying out.
  • UNII Z35I17EQOP
    A waxy substance made from glycerin and stearic acid that helps stabilize and thicken cosmetic and pharmaceutical formulations. It works as an emulsifier to blend oil and water-based ingredients together.
  • UNII YXH47AOU0F
    A synthetic fatty acid used as a thickener and stabilizer in medicines. It helps create the right texture and prevents separation of ingredients in liquid or semi-solid formulations.
  • UNII 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 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 75356789IW
    A natural ingredient derived from apricot seeds. It may serve as a filler, thickener, or texture agent in formulations.
  • UNII 8N0K3807ZW
    A natural plant extract from the bark of the quillaja tree. Used as an emulsifier and foaming agent to help mix water and oil-based ingredients together in liquid formulations.
  • UNII WUB68Y35M7
    Rose oil is a fragrant essential oil extracted from rose petals. It's used in medicines as a flavoring and scent agent to improve taste and smell.
  • 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 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 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII 65A9F4P024
    A synthetic compound derived from the amino acid glutamate and stearic acid. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients, keeping the medicine uniform throughout.
  • 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 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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 06YD7896S3
    A waxy, fatty substance derived from stearic acid. It acts as a thickener and texture modifier in medicines, helping control how quickly the drug dissolves and improving the product's firmness and consistency.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII V038D626IF
    A plant extract from Withania somnifera root, traditionally used in herbal preparations. It may function as an active botanical ingredient or filler in formulations, though its primary role depends on the specific product formulation.
  • 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.

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

The official label also statesAloe Barbadensis Leaf Juice*, C10-18 Triglycerides, Caprylic/Capric Triglyceride, Glycerin (Vegetal), Propanediol, Coco-Caprylate/Caprate, Silica, Polyglyceryl-6 Distearate, Polyhydroxystearic Acid, Sodium Citrate, Citric Acid, Glyceryl Stearate, Sodium Hyaluronate, Aesculus Hippocastanum (Horse Chestnut) Extract, Acmella Oleracea Extract, Fagus Sylvatica Bud Extract, Ascorbyl Glucoside (Vitamin C), Withania Somnifera Root Extract, Camellia Sinensis Leaf Extract, Coffea Arabica (Coffee) Leaf/Seed Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Cinnamomum Cassia Bark Extract, Rose Extract, Prunus Armeniaca (Apricot) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Glycine Soja (Soybean) Oil, Eugenia Caryophyllus (Clove) Flower Extract, Cucumis Melo Cantalupensis Fruit Extract, Orchis Mascula Flower Extract, Cananga Odorata Flower Extract, Jojoba Esters, Sodium Stearoyl Glutamate, Xanthan Gum, Salicylic Acid, Polyglyceryl-3 Beeswax, Cetyl Alcohol, Tocopherol (Vitamin E), Octyldodecanol, Parfum (Natural), Benzyl Alcohol, Trihydroxystearin, Potassium Sorbate, Alumina, Stearic Acid, Cananga Odorata Flower Oil*, Sorbic Acid, Citrus Medica Limonum (Lemon) Peel Oil*, Water (Aqua), Kigelia Africana Fruit Extract, Quillaja Saponaria Bark Extract, Alpha-Glucan Oligosaccharide, Glycogen, Fructose, CI 77891, CI 77492, CI 77491, CI 77499. *Certified organic.

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

LabelerLABORATOIRES DRUIDE INC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code71447
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from LABORATOIRES DRUIDE INC labeler code 71447

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 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 106 words ▾

Directions ▪ Apply liberally and evenly 15 minutes before sun exposure ▪ Reapply ▪ After 80 minutes of swimming or sweating ▪ Immediately after towel drying ▪ At least every 2 hours ▪ 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 ▪ Use a water-resistant sunscreen if swimming or sweating.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 9 words ▾

Active Ingredients Titanium Dioxide (Non-Nano) 2% Zinc Oxide 18.4%

🧪 Inactive Ingredients 162 words ▾

Inactive Ingredients Aloe Barbadensis Leaf Juice*, C10-18 Triglycerides, Caprylic/Capric Triglyceride, Glycerin (Vegetal), Propanediol, Coco-Caprylate/Caprate, Silica, Polyglyceryl-6 Distearate, Polyhydroxystearic Acid, Sodium Citrate, Citric Acid, Glyceryl Stearate, Sodium Hyaluronate, Aesculus Hippocastanum (Horse Chestnut) Extract, Acmella Oleracea Extract, Fagus Sylvatica Bud Extract, Ascorbyl Glucoside (Vitamin C), Withania Somnifera Root Extract, Camellia Sinensis Leaf Extract, Coffea Arabica (Coffee) Leaf/Seed Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Cinnamomum Cassia Bark Extract, Rose Extract, Prunus Armeniaca (Apricot) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Glycine Soja (Soybean) Oil, Eugenia Caryophyllus (Clove) Flower Extract, Cucumis Melo Cantalupensis Fruit Extract, Orchis Mascula Flower Extract, Cananga Odorata Flower Extract, Jojoba Esters, Sodium Stearoyl Glutamate, Xanthan Gum, Salicylic Acid, Polyglyceryl-3 Beeswax, Cetyl Alcohol, Tocopherol (Vitamin E), Octyldodecanol, Parfum (Natural), Benzyl Alcohol, Trihydroxystearin, Potassium Sorbate, Alumina, Stearic Acid, Cananga Odorata Flower Oil*, Sorbic Acid, Citrus Medica Limonum (Lemon) Peel Oil*, Water (Aqua), Kigelia Africana Fruit Extract, Quillaja Saponaria Bark Extract, Alpha-Glucan Oligosaccharide, Glycogen, Fructose, CI 77891, CI 77492, CI 77491, CI 77499. *Certified organic.

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 8 words ▾

Do not use on damaged or broken skin.

📄 When Using This Product 4 words ▾

When using this product

📄 Stop Use and Ask a Doctor If 9 words ▾

Stop use and ask a doctor if rash occurs.

📄 Keep Out of Reach of Children 18 words ▾

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

📄 Questions or Comments 8 words ▾

Questions or Comments? Call 1-800-263-8888 or visit www.nellydevuyst.com

📄 Package Label / Principal Display Panel 12 words ▾

NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 30mL (NDC 71447-033-00) Nelly_Devuyst_Biosolar_Color_Lift_3_Tinted_Sunscreen_Airless_Pump_30ml

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 NELLY DEVUYST BIOSOLAR COLORLIFT 3 TINTED SUNSCREEN SPF30 (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

Death204
Disabling32
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 270 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by LABORATOIRES DRUIDE INC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
LABORATOIRES DRUIDE INC 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.
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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.