WEN SixThirteen SPF 20 Dry Oil Intensive Treatment Octocrylene, Homosalate, Ethylhexyl Methocinnamate, Ethylhexyl Salicylate, Benzophenone 7.5 g/100mL; 4 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Spray, 200 mL — NDC 87588-0100-07 package photo

WEN SixThirteen SPF 20 Dry Oil Intensive Treatment Octocrylene, Homosalate, Ethylhexyl Methocinnamate, Ethylhexyl Salicylate, Benzophenone 7.5 g/100mL; 4 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Spray, 200 mL

by WEN by Chaz Dean · 200 mL in 1 BOTTLE, SPRAY (87588-100-07)
NDC 87588-0100-07
🏷️ FDA NDC (as labeled) 87588-100-07 billing pads the product segment with a zero
This package
Contains200 mL Pack sizes2 compare ↓
Also comes in: 89 ml 87588-0100-03
OTC On market Non-controlled
🗂️ Data synced Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 87588-100-07
Product NDC 87588-100
11-digit billing NDC 87588010007
UNII 4Y5P7MUD51, 95OOS7VE0Y, 5A68WGF6WM, V06SV4M95S, 4X49Y0596W
Application # M020
SPL Set ID 536e6291-f5ca-37a4-e063-6394a90adfdb
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-04-01
Route TOPICAL
Dosage form SPRAY
Substance ETHYLHEXYL METHOXYCINNAMATE; BENZOPHENONE-3; OCTOCRYLENE; HOMOSALATE; ETHYLHEXYL SALICYLATE
Why two NDCs? The FDA registers this code as 87588-100-07 — 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 → 87588-0100-07. 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

LabelerWEN by Chaz Dean
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code87588
First marketedApr 2019
Product typeHuman Otc Drug
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 spray sunscreen marketed as an OTC monograph product. It contains five UV-filtering agents (octocrylene, homosalate, ethylhexyl methoxycinnamate, ethylhexyl salicylate, and benzophenone-3) that are commonly used to absorb or reflect ultraviolet light from the sun. The product is labeled with an SPF 20 rating and is formulated as a dry oil spray intended for topical application to the skin.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII OF5P57N2ZX
    Alanine is a naturally occurring amino acid used in medicines as a buffering agent and pH stabilizer. It helps maintain the proper acidity level in liquid formulations to improve stability and taste.
  • 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 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 TRW2FUF47H
    A plant-derived powder from marshmallow root used as a binder and thickener in medicines. It helps hold ingredients together and can soothe irritated surfaces in throat lozenges and syrups.
  • UNII 94ZLA3W45F
    Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
  • UNII OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII H7UGK1GJCU
    Aspalathus linearis leaf is a plant extract from rooibos tea. It's used in medicines as a natural flavor and color agent, and may help preserve the product's stability.
  • UNII 30KYC7MIAI
    Aspartic acid is an amino acid used in pharmaceutical formulations as a pH buffer and to help stabilize active ingredients. It works to maintain the proper acidity level in the medicine.
  • 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • 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 NJO720F72R
    Mandarin oil is a natural essential oil extracted from mandarin orange peel. It's used as a flavor and aroma agent to make medicines taste and smell more pleasant.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • 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 S3KFG6Q5X8
    An organic chemical compound used as a UV filter in topical formulations. It helps protect the medicine or product from degradation caused by sunlight exposure during storage and use.
  • 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 Z0W6766A2W
    Acai oil is a plant-derived oil extracted from acai berries. In medicines, it serves as an emollient and carrier oil to help dissolve or distribute active ingredients and improve product texture and absorption.
  • UNII TE7660XO1C
    Glycine is an amino acid used in medicines as a buffer to help stabilize pH and improve taste. It may also serve as a filler or binder to give the product proper form and consistency.
  • UNII 4QD397987E
    An amino acid used as a buffer and stabilizer in medications. It helps maintain the pH balance and protects the active drug from breaking down during storage and use.
  • UNII 1394NXB9L6
    A plant-derived protein from soybeans that has been broken down into smaller pieces using enzymes. It acts as a binder and texture agent, helping hold ingredients together and improve the product's consistency and mouthfeel.
  • 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 04Y7590D77
    A naturally occurring amino acid used as a buffering agent and pH stabilizer in medications. It helps maintain the chemical balance of the formulation to protect drug stability.
  • UNII 72O054U628
    Lemon peel is a natural plant material from citrus fruit used as a flavoring agent and colorant in medicines. It adds tartness and a pale yellow tint to make the medication more pleasant to taste and look at.
  • UNII 930626MWDL
    A plant extract from goji berries used as a natural coloring agent and flavor enhancer in medicines. It may add color and taste while serving as a source of beneficial plant compounds in the formulation.
  • UNII 2U0KZP0FDW
    Basil is a plant-derived flavoring ingredient. It's added to medicines to improve taste and mask bitter or unpleasant flavors, making the medication easier to take.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII Q41S464P1R
    A synthetic peptide (short protein-like molecule) used in skincare and cosmetic formulations as an active conditioning ingredient to help improve skin texture and appearance. It may function as a humectant or skin-conditioning agent in topical products.
  • UNII RV743D216M
    A synthetic peptide derived from fatty acids and amino acids. It functions as a skin-conditioning agent and emollient in topical formulations, helping soften and smooth the product texture while supporting skin hydration.
  • 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 47E5O17Y3R
    Phenylalanine is an amino acid used as a sweetener and flavor enhancer in medicines and supplements. It helps make products taste better while keeping them shelf-stable.
  • UNII A034SE7857
    Phytonadione is a form of vitamin K, a naturally occurring compound. It's used in medicines as an active pharmaceutical ingredient to support blood clotting, though it may also serve as a colorant or stabilizer in some formulations.
  • UNII 9DLQ4CIU6V
    Proline is an amino acid used in pharmaceutical formulations as a bulking agent and stabilizer. It helps maintain product stability and can improve the texture or consistency of medicines, particularly in powders and freeze-dried products.
  • UNII FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to help protect the product from spoilage.
  • UNII 452VLY9402
    Serine is an amino acid, a building block of proteins. In medications, it functions as a buffering agent and stabilizer to help maintain the product's pH balance and protect active ingredients during storage.
  • 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 GH42T47V24
    A plant extract from tea leaves that acts as an antioxidant and flavor ingredient. It helps preserve the medicine and improve its taste.
  • UNII 2ZD004190S
    Threonine is an amino acid, a naturally occurring protein building block. It functions as a buffering agent and pH stabilizer in medicines to maintain proper acidity levels and product stability.
  • UNII HG18B9YRS7
    Valine is an amino acid, one of the building blocks of proteins. In medicines, it acts as a filler and bulking agent to give the product proper volume and texture.
  • UNII Q74T35078H
    Vanilla is a flavoring ingredient extracted from vanilla orchid beans. It's added to medicines to improve taste and make them more pleasant to take, especially for children or patients who need liquid formulations.
  • UNII CHI530446X
    Vanillin is a natural or synthetic aromatic compound that gives vanilla flavor. It's used in medicines as a flavoring agent to mask bitter tastes and improve how the medicine tastes.
  • UNII 035MV9S1C3
    A plastic-like polymer made from two chemical compounds joined together. It acts as a binder and film-former in tablets and capsules, helping hold ingredients together and create a protective coating on the medicine's surface.
  • UNII O0M3396E09
    White tea is a plant-derived ingredient made from tea leaves. It may be used in medicines as a flavoring agent or for its antioxidant properties to help preserve the product's stability.

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

The official label also statesisododecane, cyclopentasiloxane, c12-c15 alkyl benzoate, sd alcohol 40b, dimethicone, ethylhexyl methoxycrylene, pvp, vp/eicosene copolymer, phenyltrimethicone, olive fruit oil, lemon peel oil, lemon peel extract, rosemary leaf oil, rosemary leaf extract, vanilla planifolia fruit extract, vanillin, basil leaf extract, aloe vera leaf extract, goji fruit extract, acai fruit extract, vitamin k, arnica montana flower extract, green tea leaf extract, white tea leaf extract, roobios red tea extract, black tea leaf extract, marsh mallow/ althea extract, mandarin orange peel extract, tocopheryl acetate, palmitoyl tripeptide-1, palmitoyl tetrapeptide-7, l-valine, l-threonine, l-proline, l-isoleucine, l-phenylalanine, l-histadine, l-alanine, l-serine, l-arginine, l-aspartic acid, glycine, sodium pca, hydrolyzed soy protein, fragrance, phenoxyethanol, ethylhexylglycerin

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 DailyMedingredient 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: 89 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
WEN SixThirteen SPF 20 Dry Oil Intensive Treatment 7.5 g/100mL; 4 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mLthis 87588-0100-07 WEN 200 ml 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

🏛️
2019
On the market since
Apr 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
87588-0100-03 89 mL in 1 BOTTLE, SPRAY (87588-100-03) 2025-06-01 Active
87588-0100-07 You're viewing this 200 mL in 1 BOTTLE, SPRAY (87588-100-07) 2019-04-01 Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 87588-0100-07?
NDC 87588-0100-07 contains 200 mL — 200 ml in 1 bottle, spray.
What is the difference between NDC 87588-0100-07 and NDC 87588-0100-03?
Both are WEN SixThirteen SPF 20 Dry Oil Intensive Treatment Octocrylene, Homosalate, Ethylhexyl Methocinnamate, Ethylhexyl Salicylate, Benzophenone 7.5 g/100mL; 4 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Spray — the drug itself is identical. NDC 87588-0100-07 is the 200 mL package, while NDC 87588-0100-03 is the 89 ml package.
What NDC number is used to bill for this package of WEN SixThirteen SPF 20 Dry Oil Intensive Treatment Octocrylene, Homosalate, Ethylhexyl Methocinnamate, Ethylhexyl Salicylate, Benzophenone 7.5 g/100mL; 4 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL Spray?
Bill NDC 87588-0100-07 — the 11-digit billing format is 87588010007. 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 87588-100-07, 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: 87588-0100-07, written without dashes as 87588010007. 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 87588-0100-07, the first segment (87588) is the labeler code FDA assigned to WEN by Chaz Dean; the middle segment (0100) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (07) 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 WEN by Chaz Dean. 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 89 ml (87588-0100-03). 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?
WEN by Chaz Dean 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 28 words

Uses helps prevent sunburn if used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early aging caused by the sun

⏱️ Dosage and Administration 27 words

Directions Shake well before use. Spray liberally onto skin 15 minutes before sun exposure and spead evenly with hands. Reapply every 2 hours and immediately after swimming.

⚠️ Warnings 42 words

Warnings For external use only. Do not use on damaged or broken skin Avoid contact with eyes. If contact occurs, flush eyes thoroughly with cool water. If adverse reaction occusrs, discontinue use and ask a physician Keep out of reach of children.

🧪 Active Ingredient 14 words

Active Ingredients Octocrylene 10% Homosalate 10% Ethylhexyl Methocinnamate 7.5% Ethylhexyl Salicylate 5% Benzophenone-3 4%

🧪 Inactive Ingredients 106 words

Inactive ingredients isododecane, cyclopentasiloxane, c12-c15 alkyl benzoate, sd alcohol 40b, dimethicone, ethylhexyl methoxycrylene, pvp, vp/eicosene copolymer, phenyltrimethicone, olive fruit oil, lemon peel oil, lemon peel extract, rosemary leaf oil, rosemary leaf extract, vanilla planifolia fruit extract, vanillin, basil leaf extract, aloe vera leaf extract, goji fruit extract, acai fruit extract, vitamin k, arnica montana flower extract, green tea leaf extract, white tea leaf extract, roobios red tea extract, black tea leaf extract, marsh mallow/ althea extract, mandarin orange peel extract, tocopheryl acetate, palmitoyl tripeptide-1, palmitoyl tetrapeptide-7, l-valine, l-threonine, l-proline, l-isoleucine, l-phenylalanine, l-histadine, l-alanine, l-serine, l-arginine, l-aspartic acid, glycine, sodium pca, hydrolyzed soy protein, fragrance, phenoxyethanol, ethylhexylglycerin

🎯 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 ↗
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.