Home › NDC Lookup › Ingredients › Avobenzone, Octisalate And Octocrylene › 51150-0726-06
Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen Avobenzone, Octisalate and Octocrylene 30 mg/g; 50 mg/g; 70 mg/g Cream — NDC 51150-0726-06 package photo

Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen Avobenzone, Octisalate and Octocrylene 30 mg/g; 50 mg/g; 70 mg/g Cream

by SICOS ET CIE · 1 JAR in 1 CARTON (51150-726-06) / 15 g in 1 JAR
NDC 51150-0726-06
🏷️ FDA NDC (as labeled) 51150-726-06 billing pads the product segment with a zero
This package
Contains15 g in 1 jar Pack sizes6 compare ↓
Also comes in: 50 g 51150-0726-01 1 g 51150-0726-03 75 g 51150-0726-04 30 g 51150-0726-05 5 g 51150-0726-02
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 51150-726-06
Product NDC 51150-726
11-digit billing NDC 51150072606
UNII G63QQF2NOX, 4X49Y0596W, 5A68WGF6WM
Application # M020
SPL Set ID d8449209-65d0-43c6-8750-0f460a950157
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2019-10-28
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 51150-726-06 — 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 → 51150-0726-06. 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

LabelerSICOS ET CIE
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code51150
First marketedOct 2019
Product typeHuman Otc Drug
Portfolio26 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 topical cream marketed as an over-the-counter sunscreen under FDA's OTC monograph rules. It contains three UV-filter ingredients (avobenzone, octisalate, and octocrylene) that work together to absorb and scatter ultraviolet radiation, typically used to help protect skin from sun damage and reduce the risk of sunburn. The product is formulated with a broad-spectrum SPF 30 rating, meaning it is intended to block both UVA and UVB rays.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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 AU6XZE9IY9
    A natural wax derived from acacia decurrens flowers. It functions as a coating agent, lubricant, and polish to give tablets and capsules a smooth, protective finish and improve handling during manufacturing.
  • UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 OEB4R3WW9C
    A silicone-based emulsifier and anti-foaming agent derived from polyethylene glycol. It helps prevent foam formation during manufacturing and aids in blending oil and water components in liquid formulations.
  • UNII 5F7PJF6AA4
    A fatty acid derivative that combines salicylic acid with a plant-derived oil component. It acts as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 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 U14A832J8D
    Cinnamic acid is a naturally occurring organic compound derived from cinnamon and other plants. It functions as a preservative and flavoring agent in medicines, helping extend shelf life and add taste.
  • 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 G65ROR2RKA
    A plant extract from tree fern leaves, used as a natural thickener, emulsifier, or texture agent in formulations to help create the desired consistency and stability of the medicine.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • 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 H895X08VNQ
    A silicone-based polymer that forms small, hard particles. It acts as a glidant and anti-caking agent to improve powder flow and prevent clumping in tablets and capsules.
  • UNII OSA9UP217S
    Dimethiconol is a silicone-based lubricant and anti-foaming agent. It reduces friction between tablet components and prevents foam formation during manufacturing and storage.
  • UNII 45ASM2L11M
    A synthetic ingredient derived from glutamic acid and stearic acid. It acts as an emulsifier and surfactant, helping oils and water mix smoothly in the medication formulation.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • 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 TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII 12133JR80S
    Guanosine is a natural nucleoside compound derived from nucleic acids. In medicines, it may serve as a buffer or pH regulator to help stabilize the formulation and maintain proper acidity levels.
  • 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 UDR641JW8W
    A plant-derived oil from jojoba seeds that has been broken down into smaller components. It acts as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII QQC1AK06RK
    A botanical extract from alpine edelweiss flowers used as a natural fragrance, flavor component, or skin-conditioning agent in topical or oral formulations. It may also serve antioxidant or soothing purposes in finished products.
  • UNII RYX5QG61EI
    Levulinic acid is an organic compound derived from cellulose that acts as a buffer and pH regulator in medications. It helps maintain stable acidity levels in the formulation.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • UNII 412ZHA4T4Y
    A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
  • UNII 762O8IWA10
    PEG-8 laurate is a synthetic compound made by combining polyethylene glycol with lauric acid. It acts as an emulsifier and solubilizer in medicines, helping to blend water and oil-based ingredients together and improve how well some drugs dissolve.
  • 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 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 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 7J95K7ID2S
    A plant extract from the roots of Chinese skullcap, used as a natural coloring agent and to add mild flavor to medicines. It may also help preserve the product's stability.
  • 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 554127163Y
    Sodium dodecylbenzenesulfonate is a synthetic detergent and surfactant used in medicines to help dissolve or suspend active ingredients and improve how the product flows and mixes during manufacturing.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII VK44E1MQU8
    Sodium levulinate is a salt derived from levulinic acid, a naturally occurring organic compound. It functions as a humectant and preservative in medicines, helping retain moisture and prevent microbial growth.
  • UNII 5Z4DPO246A
    A synthetic plastic polymer made from styrene and acrylamide monomers. It acts as a film-former and binder in tablets and capsules, helping hold ingredients together and control how quickly the medicine dissolves and releases in your body.
  • 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 9NH1UDD2RR
    A synthetic silicone polymer that forms a smooth, water-resistant film. Used in topical formulations as a skin protectant coating and to improve product texture and spreadability on the skin.
  • 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 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.

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

The official label also stateswater, glycerin, dimethicone, isononyl isononanoate, propanediol, vinyl dimethicone/methicone silsesquioxane crosspolymer, alcohol denat., bis-PEG-18 methyl ether dimethyl silane, polyglyceryl-6 distearate, jojoba esters, tocopherol, limnanthes alba (meadowfoam) seed oil, acacia decurrens flower wax, guanosine, cyathea medullaris leaf extract, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, sodium levulinae, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurae/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolyer, dimethiconol, limonene, xanthan gum, benzyl alcohol, cinnamic acid, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, sculellaria baicalensis root extract, levulinic acid, styrene/acrylaes copolymer, clyberyl caprylate, fragrance

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 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: 50 g 1 g 75 g 30 g 5 g
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
Lancome Paris Visionnaire Broad Spectrum SPF 20 Sunscreen Advanced Multi Correcting All Skin Types 30 mg/g; 50 mg/g; 70 mg/g 49967-0194-01 L'Oreal 1 jar — — Discontinued —
Lancome Paris Bienfait MultiVital Broad Spectrum SPF 30 Sunscreen 30 mg/g; 50 mg/g; 70 mg/g 49967-0456-01 L'Oreal 1 jar — — FDA listed —
Lancome Paris Renergie Lift MultiAction Sunscreen Broad Spectrum SPF 15 Lift and Firming Face and Neck All Skin Types 30 mg/g; 50 mg/g; 70 mg/g 49967-0633-01 L'Oreal 1 jar — — FDA listed —
Lancome Paris Bienfait MultiVital Eye Broad Spectrum SPF 30 Sunscreen 30 mg/g; 50 mg/g; 70 mg/g 49967-0878-01 L'Oreal 1 tube — — FDA listed —
Lancome Paris Renergie Lift MultiAction Sunscreen Broad Spectrum SPF 15 Lift Firming Face Neck For All Skin Types 30 mg/g; 50 mg/g; 70 mg/g 51150-0634-01 SICOS 1 jar — — FDA listed —
Lancome Paris Renergie HPN 300 Peptide Broad Spectrum SPF 25 Sunscreen 30 mg/g; 50 mg/g; 70 mg/g 51150-0240-01 SICOS 1 jar — — FDA listed —
Lancome Paris Renergie HPN 300 Peptide Broad Spectrum SPF 25 Sunscreen 30 mg/g; 50 mg/g; 70 mg/g 49967-0240-01 L'Oreal 1 jar — — FDA listed —
Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen 30 mg/g; 50 mg/g; 70 mg/g 49967-0726-01 L'Oreal 1 jar — — FDA listed —
Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen 30 mg/g; 50 mg/g; 70 mg/gthis 51150-0726-06 SICOS 1 jar — — Discontinued —
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

🏛️
2019
On the market since
Oct 2019
📍
2026
Currently FDA-listed
7 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
51150-0726-01 1 JAR in 1 CARTON (51150-726-01) / 50 g in 1 JAR 2019-10-28 Active
51150-0726-02 5 g in 1 JAR (51150-726-02) 2019-10-28 Discontinued by firm
51150-0726-03 1 g in 1 PACKET (51150-726-03) 2019-10-28 Discontinued by firm
51150-0726-04 1 JAR in 1 CARTON (51150-726-04) / 75 g in 1 JAR 2019-10-28 Discontinued by firm
51150-0726-05 1 JAR in 1 CARTON (51150-726-05) / 30 g in 1 JAR 2019-10-28 Discontinued by firm
51150-0726-06 You're viewing this 1 JAR in 1 CARTON (51150-726-06) / 15 g in 1 JAR 2019-10-28 Discontinued by firm

Pack size FAQ

What quantity is in NDC 51150-0726-06?
NDC 51150-0726-06 is listed by the FDA — 1 jar in 1 carton / 15 g in 1 jar.
What NDC number is used to bill for this package of Lancome Paris Renergie Lift MultiAction Ultra Lifting Firming Dark Spot Correcting Broad Spectrum SPF 30 Sunscreen Avobenzone, Octisalate and Octocrylene 30 mg/g; 50 mg/g; 70 mg/g Cream?
Bill NDC 51150-0726-06 — the 11-digit billing format is 51150072606. 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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 51150-726-06, 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: 51150-0726-06, written without dashes as 51150072606. 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 51150-0726-06, the first segment (51150) is the labeler code FDA assigned to SICOS ET CIE; the middle segment (0726) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (06) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 1 jar (51150-0726-01), 1 g (51150-0726-03), 1 jar (51150-0726-04). 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?
SICOS ET CIE 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 30 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 105 words ▾

Directions For sunscreen use: ● apply generously and evenly 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 5 words ▾

Warnings For external use only

📦 Storage and Handling 14 words ▾

Other information protect the product in this container from excessive heat and direct sun

🧪 Active Ingredient 8 words ▾

Active ingredients Avobenzone 3% Octisalate 5% Octocrylene 7%

🧪 Inactive Ingredients 112 words ▾

Inactive ingredients water, glycerin, dimethicone, isononyl isononanoate, propanediol, vinyl dimethicone/methicone silsesquioxane crosspolymer, alcohol denat., bis-PEG-18 methyl ether dimethyl silane, polyglyceryl-6 distearate, jojoba esters, tocopherol, limnanthes alba (meadowfoam) seed oil, acacia decurrens flower wax, guanosine, cyathea medullaris leaf extract, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, sodium levulinae, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurae/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolyer, dimethiconol, limonene, xanthan gum, benzyl alcohol, cinnamic acid, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, sculellaria baicalensis root extract, levulinic acid, styrene/acrylaes copolymer, clyberyl caprylate, fragrance

🎯 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 ↗
← 51150-0712-01 · SICOS 51150-0736-01 · SICOS →
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.