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Weightless Protection SPF 45 Sunscreen Broad Spectrum 2 g/100mL; 5 g/100mL; 8.4 g/100mL Lotion, 50 mL — NDC 68726-0262-11 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Weightless Protection SPF 45 Sunscreen Broad Spectrum 2 g/100mL; 5 g/100mL; 8.4 g/100mL Lotion, 50 mL — NDC 68726-262-11 (Billing 68726-0262-11)

by CP Skin Health Group, Inc. · 50 mL in 1 TUBE

This is a package of 50 mL of Weightless Protection SPF 45 Sunscreen Broad Spectrum 2 g/100mL; 5 g/100mL; 8.4 g/100mL Lotion from CP Skin Health Group, Inc., marketed since May 2020 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 68726-0262-11
🏷️ FDA NDC (as labeled) 68726-262-11 billing pads the product segment with a zero
This package
Contains50 mL Pack sizes3 compare ↓
Main listing for product 68726-262 · Also comes in: 7.4 ml 68726-262-37 195 ml 68726-262-53
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 68726-262-11 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
68726 labeler · 262 product · 11 package
Package marketed since
May 1, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6872626211 0
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 68726-262-11
Product NDC 68726-262
11-digit billing NDC 68726026211
UNII 5A68WGF6WM, 4X49Y0596W, SOI2LOH54Z
Application # M020
SPL Set ID b6bee26d-bffd-a8ee-e053-2a95a90affc5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-05-01
Route TOPICAL
Dosage form LOTION
Substance OCTOCRYLENE; OCTISALATE; ZINC OXIDE
Why two NDCs? The FDA registers this code as 68726-262-11 — 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 → 68726-0262-11. 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?

Weightless Protection SPF 45 is a topical lotion sunscreen marketed as an over-the-counter monograph product. It contains three active ingredients that work together to protect skin from ultraviolet (UV) radiation: octisalate and octocrylene are organic UV filters that absorb sunlight, while zinc oxide is a mineral filter that reflects UV rays. This broad-spectrum lotion is typically used to help shield exposed skin from both UVA and UVB sun damage when applied before sun exposure.

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.

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: 7.4 ml 195 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
68726-0262-11 You're viewing this Main listing 50 mL in 1 TUBE 2020-05-01 — Active
68726-0262-37 68726-262-37 7.4 mL in 1 TUBE 2020-05-01 — Active
68726-0262-53 68726-262-53 195 mL in 1 BOTTLE 2020-05-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 50 mL — 50 ml in 1 tube.
How does this package differ from NDC 68726-0262-37?
Both are Weightless Protection SPF 45 Sunscreen Broad Spectrum 2 g/100mL; 5 g/100mL; 8.4 g/100mL Lotion — the drug itself is identical. This page's package is the 50 mL one, while NDC 68726-0262-37 is the 7.4 ml package.
What NDC number is used to bill for this package of Weightless Protection SPF 45 Sunscreen Broad Spectrum 2 g/100mL; 5 g/100mL; 8.4 g/100mL Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Weightless Protection SPF 45 2 g/100mL; 5 g/100mL; 8.4 g/100mLthis 68726-0262-11 CP 50 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

🏛️
2020
On the market since
May 2020
📍
2026
Currently FDA-listed
6 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 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 B423VGH5S9
    A natural fruit ingredient derived from apples, used as a flavoring agent and sweetener to improve taste and palatability of the medicine.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII 3G6A5W338E
    Caffeine is a natural stimulant compound commonly extracted from coffee beans and tea leaves. In medicines, it serves as an active booster in pain relievers and cold products to enhance alertness and improve the effectiveness of other ingredients.
  • 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 Q95M2P1KJL
    A silicone-based ingredient that acts as a lubricant and glidant. It helps the tablet or capsule move smoothly through manufacturing equipment and improves powder flow during production.
  • UNII YY7C30VXJT
    A natural plant extract from cucumber that adds flavor and freshness to medicines. It may also serve as a moisturizing agent or mild preservative in topical or oral formulations.
  • 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 7GXZ3858RY
    Ectoine is a naturally derived protective compound used in pharmaceuticals as a stabilizer and humectant. It helps preserve the integrity of active ingredients and maintain moisture in formulations.
  • UNII 5B8915UELW
    A plant-derived compound used as an antioxidant in medicines. It helps prevent spoilage and degradation of active ingredients during storage by protecting them from oxidative damage.
  • 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 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 86FQE96TZ4
    A synthetic polymer, this ingredient acts as a thickener and suspending agent in liquid formulations. It helps maintain uniform consistency and keeps particles evenly distributed throughout the medicine.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 O2H83I4PUN
    A plant-derived ingredient from spearmint leaves. It adds flavor and aroma to the medicine and may help mask the taste of other ingredients.
  • UNII 79M2M2UDA9
    Mentha piperita is peppermint, a plant extract used in medicines as a flavoring agent and to provide a cooling or soothing taste. It helps make the medication more pleasant to take.
  • UNII ZV095H5633
    A natural flavoring derived from muskmelon fruit. It is used in medicines to add pleasant taste and aroma, making the product more acceptable to take.
  • UNII KQX236OK4U
    A fine powder made from the outer layer of oat grain. It acts as a filler and binder to give the medicine its form and texture, and may also help the tablet or capsule break down properly in the digestive system.
  • UNII X8725R883T
    A synthetic oily liquid derived from branched carboxylic acids, used as an emollient and skin-conditioning agent in topical formulations. It helps soften and smooth the product's texture while improving how it spreads on skin.
  • UNII 8Q0Z18J1VL
    A surfactant derived from oleic acid, a naturally occurring fatty acid. It helps mix oil and water-based ingredients together in formulations, improving product stability and texture.
  • UNII TI9T76XD44
    A natural flavoring derived from orange fruit peel. It adds orange taste and aroma to the medicine, making it more pleasant to take, while also providing natural color.
  • UNII SF206I8G4P
    A plant extract from passion fruit used in medicines as a natural flavoring agent and to add mild taste appeal to oral formulations.
  • 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 5XB3A63Y52
    A synthetic rubber polymer used as a glidant and lubricant in tablet and capsule formulations. It reduces friction between particles and equipment surfaces, helping medicines flow smoothly during manufacturing and preventing sticking.
  • 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 4N14V5R27W
    A natural flavoring derived from raspberry fruit that gives medicines a pleasant taste. It helps mask bitter or unpleasant flavors to make medications easier to swallow.
  • UNII 3641YW25N2
    A fragrant oil extracted from sandalwood tree wood, used as a flavoring agent and fragrance to improve the taste and smell of medicines.
  • UNII U946SH95EE
    Milk thistle is a plant extract used in some supplements and herbal formulations. It may act as an active botanical ingredient rather than a traditional inactive excipient, though it can also serve as a filler or binder in tablet or capsule preparations.
  • 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 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 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 HA26P2LA4P
    A silicone polymer that creates a smooth, protective barrier on the skin. It acts as an emollient and film-former to improve product texture, spreadability, and water resistance in topical formulations.
  • 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.

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

The official label also statesAvena Sativa (Oat) Bran Extract Bisabolol Butylene Glycol Butyloctyl Salicylate Caffeine Caprylic/Capric Triglyceride Caprylyl Methicone Citrus Aurantium Dulcis (Orange) Peel Extract Cucumis Melo Cantalupensis Fruit Extract Cucumis Melo (Melon) Fruit Extract Cucumis Sativus (Cucumber) Fruit Extract Cyclopentasiloxane Dimethicone Ectoin Ethyl Ferulate Ethylhexylglycerin Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Mentha Piperita (Peppermint) Extract Mentha Viridis (Spearmint) Extract Octyldodecyl Neopentanoate Oleth-3 Phosphate Passiflora Incarnata Fruit Extract PEG-7 Trimethylolpropane Coconut Ether Phenoxyethanol Polyisobutene Propanediol Pyrus Malus (Apple) Fruit Extract Rubus Idaeus (Raspberry) Fruit Extract Rose Extract Santalum Album (Sandalwood) Wood Extract Silybum Marianum Seed Extract Sodium Hyaluronate Sodium Stearoyl Glutamate Styrene/Acrylates Copolymer Tocopheryl Acetate Triethoxycaprylylsilane Undecylcrylene Dimethicone Water

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

LabelerCP Skin Health Group, Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code68726
First marketedMay 2020
Product typeHuman Otc Drug
Portfolio31 products on file

More NDCs from CP Skin Health Group, Inc. labeler code 68726

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 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 words ▾

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

⏱️ Dosage and Administration 92 words ▾

Directions Apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating Reapply at least every two hours Children under 6 months: ask a doctor Sun Protectin 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 skin protecting measures including: limit time in the sun, especially from 10 a.m. - 2 p.m., wear long sleeved shirts, pants, hats and sunglasses.

⚠️ Warnings 57 words ▾

Warnings For external use only. Do not use on damaged or broken skin. Stop use and ask a doctor if skin rash occurs. When using this product keep out of eyes. Rinse with water to remove Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 11 words ▾

Active Ingredients Octisalate (4.9%) Octocrylene (1.9%) Zinc Oxide (8.4%) Purpose Sunscreen

🧪 Inactive Ingredients 106 words ▾

Inactive Ingredients Avena Sativa (Oat) Bran Extract Bisabolol Butylene Glycol Butyloctyl Salicylate Caffeine Caprylic/Capric Triglyceride Caprylyl Methicone Citrus Aurantium Dulcis (Orange) Peel Extract Cucumis Melo Cantalupensis Fruit Extract Cucumis Melo (Melon) Fruit Extract Cucumis Sativus (Cucumber) Fruit Extract Cyclopentasiloxane Dimethicone Ectoin Ethyl Ferulate Ethylhexylglycerin Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer Mentha Piperita (Peppermint) Extract Mentha Viridis (Spearmint) Extract Octyldodecyl Neopentanoate Oleth-3 Phosphate Passiflora Incarnata Fruit Extract PEG-7 Trimethylolpropane Coconut Ether Phenoxyethanol Polyisobutene Propanediol Pyrus Malus (Apple) Fruit Extract Rubus Idaeus (Raspberry) Fruit Extract Rose Extract Santalum Album (Sandalwood) Wood Extract Silybum Marianum Seed Extract Sodium Hyaluronate Sodium Stearoyl Glutamate Styrene/Acrylates Copolymer Tocopheryl Acetate Triethoxycaprylylsilane Undecylcrylene Dimethicone Water

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Other Information 11 words ▾

Other Information Protect this product from excessive heat and direct sun

📄 Questions or Comments 4 words ▾

Questions Please call 877.722.7546

📄 Recent Major Changes 29 words ▾

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

📄 Package Label / Principal Display Panel 4 words ▾

Weightless Protection Weightless Protection

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 CP Skin Health Group, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 7.4 ml (68726-0262-37), 195 ml (68726-0262-53). 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?
CP Skin Health Group, 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.
← 68726-0169-04 · CP 68726-0263-11 · CP →
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.