ALPET E3 HAND SANITIZER FOAM ALCOHOL 62 mL/100mL Liquid, 208197 mL
by Best Sanitizers, Inc. · 208197 mL in 1 DRUM (59900-125-02)
NDC 59900-0125-02
🏷️ FDA NDC (as labeled)
59900-125-02
billing pads the product segment with a zero
This package
Contains208197 mL
Pack sizes4 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
59900-125-02
Product NDC
59900-125
11-digit billing NDC
59900012502
RxCUI
616763
UNII
3K9958V90M
Application #
505G(a)(3)
SPL Set ID
53573e1a-a3f8-4598-8248-ec4a62392d00
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2019-05-01
Route
TOPICAL
Dosage form
LIQUID
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 59900-125-02 — 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 → 59900-0125-02. 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.
🏷️ RxNorm drug class
This medicine belongs to the Other antiseptics and disinfectants class.
Drug family (ATC)
Other antiseptics and disinfectants, Antidotes, Nerve depressants
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.
🏭 Manufacturer & labeler
LabelerBest Sanitizers, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code59900
First marketedMay 2019
Product typeHuman Otc Drug
Portfolio14 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
📗 Our plain-language guide HelloPharmacist
- Chemically they are related, but hand sanitizer is absolutely not safe to drink — it contains alcohol in concentrations that are toxic if swallowed and often includes other ingredi...
- Is the alcohol in hand sanitizer the same as the alcohol in a drink?
- Yes — most of these products are specifically labeled 'recommended for repeated use.' Just apply enough to cover your hands and rub until dry. If you notice skin irritation or redn...
- Can I use hand sanitizer over and over throughout the day?
Patient education
Supplement & herbal interactions
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.
💬 Questions about ALCOHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 4YK5Z54AT2
Denatonium benzoate is a bitter-tasting chemical compound added to medicines to discourage accidental ingestion, especially by children. It serves as a bittering agent with no therapeutic effect on the body.
-
UNII 4J55VM509S
A synthetic compound made from diethanolamine and perfluorinated alkyl phosphates. It functions as a surfactant and emulsifier, helping to blend oil and water-based ingredients together in the formulation.
-
UNII JWM00VS7HC
A plant-derived emulsifier made from coconut oil and glycerin. It helps blend oil and water-based ingredients together and improves how the medicine spreads or absorbs into skin.
-
UNII MD83SFE959
A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
-
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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive Ingredients Water, DEA-C8-18 perfluoroalkylethyl phosphate, glycereth-2 cocoate, denatonium benzoate, tert-butyl alcohol
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 system | Per mL | Per 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
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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Alcare OR Foamed Antiseptic Handrub 62 g/100g 11084-0802-80 | SC | 482 g | — | — | FDA listed | — |
| Alcare Plus Foamed Antiseptic Handrub 62 g/100g 11084-0803-36 | SC | 255 g | — | — | FDA listed | — |
| FoamFresh Alco-Foam Hand Sanitizer 62 mL/100mL 11429-1004-00 | Woodbine | 400 ml | — | — | FDA listed | — |
| Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic 62 mL/100mL 23667-0104-00 | Formulated | 222 ml | — | — | Discontinued | — |
| Symmetry Foaming Hand Sanitizer 62 mL/100mL 30805-0003-03 | Buckeye | 2000 ml | — | — | FDA listed | — |
| Symmetry Foaming Hand Sanitizer-Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0009-04 | Buckeye | 1200 ml | — | — | FDA listed | — |
| Altra Foaming Hand Sanitizer with Aloe and Vitamin E 62 mL/100mL 30805-0012-04 | Buckeye | 1200 ml | — | — | FDA listed | — |
| Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0013-04 | Buckeye | 1200 ml | — | — | FDA listed | — |
| Hand Guard Foaming Alcohol Instant Hand Sanitizer 620 mL/L 31507-0024-24 | Wechem, | 1 l | — | — | FDA listed | — |
| Hand Guard Foaming Instant Hand Sanitizer .62 mL/mL 31507-0585-08 | Wechem, | 1000 ml | — | — | FDA listed | — |
| Ecolab 62 mL/100mL 47593-0472-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL 50865-0688-09 | Kutol | 3785 ml | — | — | FDA listed | — |
| Amcon Labs Hand Sanitizer Instant Foam Sanitizer with Alcohol 620 mL/L 51801-0366-18 | Nomax, | 55 l | — | — | FDA listed | — |
| Scott Moisturizing Foam Hand Sanitizer 62 mL/100mL 55118-0546-63 | Kimberly-Clark | 6 bottles | — | — | FDA listed | — |
| Foaming Mousse Anti-Bacterial Hand Sanitizer Cherry Scented 62 mL/100mL 56136-0021-01 | Ganzhou | 50 ml | — | — | FDA listed | — |
| Foaming Mousse Anti-Bacterial Hand Sanitizer Pineapple Scented 62 mL/100mL 56136-0022-01 | Ganzhou | 50 ml | — | — | FDA listed | — |
| Foaming Mousse Anti-Bacterial Hand Sanitizer Pink Grapefruit Scented 62 mL/100mL 56136-0023-01 | Ganzhou | 50 ml | — | — | FDA listed | — |
| Alpet E3 Hand Sanitizer Foam 62 mL/100mLthis 59900-0125-02 | Best | 208197 ml | — | — | FDA listed | — |
| Simple Hygiene foaming hand Sanitizer 62 .62 mL/mL 60933-0062-01 | FULLER | 1000 ml | — | — | FDA listed | — |
| Simple Hygiene Hand Sanitizer 620 mg/mL 60933-0220-00 | FULLER | 1000 ml | — | — | FDA listed | — |
| Foaming Alcohol Hand Sanitizer .62 mL/mL 63900-0002-00 | Simoniz | 1000 ml | — | — | FDA listed | — |
| Soft Care Foam Instant Hand Sanitizer 62 mL/100mL 64536-7295-04 | Diversey, | 532 ml | — | — | FDA listed | — |
| WhiskCare 373 620 mL/L 65585-0374-01 | Whisk | 1 l | — | — | Discontinued | — |
| Aire-Master Foaming Hand Sanitizer Fragrance Free 620 mL/L 65585-0524-01 | Whisk | 3.785 l | — | — | FDA listed | — |
| Avant Foaming Hand Sanitizer 62 mL/100mL 68306-0109-01 | B4 | 530 ml | — | — | FDA listed | — |
| Hand Sanitizer 62 mL/100mL 69674-0100-01 | Saraya | 500 ml | — | — | FDA listed | — |
| Servo Stat-Foam 62 mL/100mL 76378-0011-01 | Enzyme | 59 ml | — | — | FDA listed | — |
| Hillyard Foaming Instant Hand Sanitizer 62 mL/100mL 76402-0410-02 | Hillyard | 1000 ml | — | — | FDA listed | — |
| CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0000-01 | CleanGenic, | 3790 ml | — | — | FDA listed | — |
| CleanGenic 1 GALLON HAND SANITIZER 62 mL/100mL 81385-0001-04 | CleanGenic, | 24 bottles | — | — | FDA listed | — |
| CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0002-08 | CleanGenic, | 237 ml | — | — | FDA listed | — |
| CleanGenic 8 OZ HAND SANITIZER 62 mL/100mL 81385-0003-08 | CleanGenic, | 24 bottles | — | — | FDA listed | — |
| Transcend Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0001-01 | Von | 1250 ml | — | — | FDA listed | — |
| Harbor Mist Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0003-01 | Von | 1250 ml | — | — | FDA listed | — |
| Freeman Packaging Hand Sanitizer 62 mL/100mL 71734-0201-01 | JIANGMEN | 7.5 ml | — | — | FDA listed | — |
| Afassco Hand Sanitizer 62 mL/100mL 71734-0206-01 | JIANGMEN | 2 ml | — | — | FDA listed | — |
| antiseptic hand sanitizer 01 62 mL/100mL 82953-0007-01 | Cosmuses | 10 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 72288-0849-32 | Amazon.com | 354 ml | — | — | FDA listed | — |
| Symmetry Hand Sanitizer 62 mL/100mL 30805-0001-01 | Buckeye | 9 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 59450-0471-16 | The | 89 ml | — | — | Discontinued | — |
| Alcohol 62 mL/100mL 30142-0849-16 | The | 59 ml | — | — | FDA listed | — |
| Hand Sanitizer 62 mL/100mL 87001-0006-01 | HAIAN | 35 ml | — | — | FDA listed | — |
| hand sanitizer 01 62 mL/100mL 82953-0015-01 | Cosmuses | 10 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 11344-0849-16 | Nice-Pak | 59 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 41163-0826-16 | United | 59 ml | — | — | FDA listed | — |
| Antibacterial Hand Sanitizer 62 mL/100mL 82953-0001-01 | Cosmuses | 10 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 00363-0046-16 | Walgreen | 59 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 79481-0826-01 | Meijer, | 59 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 72288-0826-32 | Amazon.com | 354 ml | — | — | FDA listed | — |
| Hydrating and Moisturizing Hand Sanitizer 62 mL/100mL 75112-0010-01 | Zhejiang | 35 ml | — | — | Discontinued | — |
| Antibacterial Hand Sanitizer 62 mL/100mL 82953-0008-01 | Cosmuses | 15 ml | — | — | FDA listed | — |
| Antiseptic Hand Sanitizer 62 mL/100mL 83165-0000-00 | Hubei | 1.03 ml | — | — | FDA listed | — |
| Altra Hand Sanitizer with Aloe and Vitamin E 62 mL/100mL 30805-0014-06 | Buckeye | 59.2 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 41163-0975-16 | United | 59 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 79481-0849-01 | Meijer, | 59 ml | — | — | FDA listed | — |
| GenRx Anti-Bacterial Gel 62 mL/100mL 59088-0299-08 | PureTek | 118 ml | — | — | FDA listed | — |
| Antibacterial Hand Sanitizer 62 mL/100mL 71160-0188-12 | TEKWELD | 12 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 11673-0826-16 | Target | 59 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 55910-0889-48 | Old | 1005 ml | — | — | Discontinued | — |
| Instant Hand Sanitizer 62 mL/100mL 59898-0420-01 | Water-Jel | 1728 packets | — | — | 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
May 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.
🔬 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 ALPET E3 HAND SANITIZER FOAM (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 55%
Female · 45%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 59900-0125-02 You're viewing this | 208197 mL in 1 DRUM (59900-125-02) | 2019-05-01 | Active |
| 59900-0125-03 | 3785 mL in 1 JUG (59900-125-03) | 2019-05-01 | Active |
| 59900-0125-05 | 1250 mL in 1 BOTTLE (59900-125-05) | 2019-05-01 | Active |
| 59900-0125-08 | 250 mL in 1 BOTTLE (59900-125-08) | 2019-05-01 | Active |
You're viewing the largest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 59900-0125-02?
NDC 59900-0125-02 contains 208197 mL — 208197 ml in 1 drum.
What is the difference between NDC 59900-0125-02 and NDC 59900-0125-08?
Both are ALPET E3 HAND SANITIZER FOAM ALCOHOL 62 mL/100mL Liquid — the drug itself is identical. NDC 59900-0125-02 is the 208197 mL package, while NDC 59900-0125-08 is the 250 ml package.
What NDC number is used to bill for this package of ALPET E3 HAND SANITIZER FOAM ALCOHOL 62 mL/100mL Liquid?
Bill NDC 59900-0125-02 — the 11-digit billing format is 59900012502. 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 59900-125-02, 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: 59900-0125-02, written without dashes as 59900012502. 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 59900-0125-02, the first segment (59900) is the labeler code FDA assigned to Best Sanitizers, Inc.; the middle segment (0125) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Best Sanitizers, 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 3 other package presentations of this same product, including 250 ml (59900-0125-08), 1250 ml (59900-0125-05), 3785 ml (59900-0125-03). 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?
Best Sanitizers, 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.
📄 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 ▾
Uses sanitizes hands to help reduce bacteria that potentially can cause disease helps to prevent cross-contamination recommended for repeated use helps prevent drying of skin
⏱️ Dosage and Administration ▾
Directions receive an adequate amount of foam into palm of hand rub thoroughly over all surfaces of both hands rub hands together until dry
⚠️ Warnings ▾
Warnings For external use only Flammable, keep away from fire or flame When using this product do not use in or near eyes use in a well-ventilated area Stop use and consult a doctor if irritation or redness develop. Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately
📦 Storage and Handling ▾
Other Information store in a cool, dry place below 104 o F (40 o C)
🧪 Active Ingredient ▾
Active ingredient Alcohol 62.0%
🧪 Inactive Ingredients ▾
Inactive Ingredients Water, DEA-C8-18 perfluoroalkylethyl phosphate, glycereth-2 cocoate, denatonium benzoate, tert-butyl alcohol
🎯 Purpose ▾
Purpose Hand Sanitizer
No label section mentions that — try another word, or open the full label on DailyMed below.
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.