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Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel, 473 mL — NDC 62257-0061-47 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel, 473 mL — NDC 62257-061-47 (Billing 62257-0061-47)

by ABC Compounding Co., Inc. · 473 mL in 1 BOTTLE, PLASTIC

This is a package of 473 mL of Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel from ABC Compounding Co., Inc., marketed since Jul 2020 and currently FDA-listed.

NDC 62257-0061-47
🏷️ FDA NDC (as labeled) 62257-061-47 billing pads the product segment with a zero
This package
Contains473 mL Pack sizes10 compare ↓
Product page 62257-0061-01 Also comes in: 2.5 ml 62257-061-21 118 ml 62257-061-24 149 ml 62257-061-28 532 ml 62257-061-17 800 ml 62257-061-13 1000 ml 62257-061-11 1000 ml 62257-061-12 1200 ml 62257-061-01 3785 ml 62257-061-14
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 62257-061-47 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
62257 labeler · 061 product · 47 package
Package marketed since
Dec 4, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6225706147 1
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 62257-061-47
Product NDC 62257-061
11-digit billing NDC 62257006147
UNII 3K9958V90M
Application # M004
SPL Set ID ee46cb57-c79c-4edf-bc88-4a4f8a95bfc8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-07-20
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 62257-061-47 — 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 → 62257-0061-47. 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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

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: 2.5 ml 118 ml 149 ml 532 ml 800 ml 1000 ml 1000 ml 1200 ml 3785 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
62257-0061-01 62257-061-01 Main listing 1200 mL in 1 CARTRIDGE 2020-12-04 — Discontinued by firm
62257-0061-11 62257-061-11 1000 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Active
62257-0061-12 62257-061-12 1000 mL in 1 BAG 2020-12-04 — Discontinued by firm
62257-0061-13 62257-061-13 800 mL in 1 BAG 2020-12-04 — Discontinued by firm
62257-0061-14 62257-061-14 3785 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Active
62257-0061-17 62257-061-17 532 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Active
62257-0061-21 62257-061-21 2.5 mL in 1 DOSE PACK 2020-12-04 — Discontinued by firm
62257-0061-24 62257-061-24 118 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Discontinued by firm
62257-0061-28 62257-061-28 149 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Discontinued by firm
62257-0061-47 You're viewing this 473 mL in 1 BOTTLE, PLASTIC 2020-12-04 — Active

Pack size FAQ

What quantity is in this package?
This package contains 473 mL — 473 ml in 1 bottle, plastic.
How does this package differ from NDC 62257-0061-21?
Both are Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel — the drug itself is identical. This page's package is the 473 mL one, while NDC 62257-0061-21 is the 2.5 ml package.
What NDC number is used to bill for this package of Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel?
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
Jianerkang Sanitizing Wipe .7 mL/mL 34645-0003-01 Jianerkang 1 patch — — FDA listed —
Instant Hand Sanitizer STERILE 70 Ethyl Alcohol .7 mL/mL 34645-0007-01 Jianerkang 1 patch — — FDA listed —
Zany Antiseptic Gel .7 mL/mL 55715-0004-01 Laboratorios 120 ml — — FDA listed —
Antibacterial Hand Sanitizer .7 mL/mL 63710-0001-01 Laboratorios 500 ml — — FDA listed —
Zeyco Antiseptic Hand Sanitizer Gel .7 mL/mL 63710-0002-01 Laboratorios 125 ml — — FDA listed —
Zeyco Hand Sanitizer .7 mL/mL 63710-0003-01 Laboratorios 500 ml — — FDA listed —
Antiseptic Hand Sanitizer .7 mL/mL 63710-0004-00 Laboratorios 500 ml — — FDA listed —
Hand Sanitizer .7 mL/mL 67326-0005-00 Degasa, 118 ml — — FDA listed —
Protec Hand Sani Gel Antibacterial .7 mL/mL 67326-0006-00 Degasa, 118 ml — — FDA listed —
Degasa Hand Sanitizer Lemon Lime Scent .7 mL/mL 67326-0010-02 Degasa, 59.14 ml — — FDA listed —
Hand Sanitizer .7 mL/mL 70412-0192-36 Zhejiang 236 ml — — FDA listed —
Antibacterial Hand Sanitizer .7 mL/mL 73145-0003-01 ASC 30 ml — — FDA listed —
Antibacterial Hand Sanitizer .7 mL/mL 73145-0004-01 ASC 236 ml — — FDA listed —
AMBI Soothing Hand sanitizer .7 mL/mL 73453-0143-04 AMBI 118 ml — — FDA listed —
Instant Hand Sanitizing Gel .7 mL/mL 77462-0011-01 SORA 50 bottles — — FDA listed —
Instant Sanitizing Gel .7 mL/mL 77462-0012-01 SORA 500 ml — — FDA listed —
XPRO Antiseptic Hand Sanitizer .7 mL/mL 77939-0000-08 Savone 240 ml — — FDA listed —
Cucumber Melon Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0003-01 Fourstar 29 ml — — FDA listed —
Fresh Peach Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0004-01 Fourstar 29 ml — — FDA listed —
Ocean Breeze Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0005-01 Fourstar 29 ml — — FDA listed —
Sweet Pea Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0006-01 Fourstar 29 ml — — FDA listed —
LEMONBELLA Lavender Hand Sanitizer .7 mL/mL 81319-0112-01 Lemonbella 100.5 ml — — FDA listed —
Reddy Lab Advanced Alcohol Gel Sanitizer .7 mL/mL 79671-0797-10 Flavor 1000 ml — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6006-01 Professional 3.23 ml — — FDA listed —
CareALL Hand Sanitizer .7 mL/mL 51824-0110-02 New 59 ml — — FDA listed —
Hand-Aid .7 mL/mL 62257-0122-01 ABC 1200 ml — — Discontinued —
Han-I-Size Unscented .7 mL/mL 63533-0645-14 Momar 3785 ml — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6007-01 Professional 484 ml — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6008-01 Professional 805.44 ml — — FDA listed —
PURELL Advanced Hand Sanitizer E3 Gel .7 mL/mL 21749-0711-89 GOJO 1200 ml — — FDA listed —
Purell Advanced Soothing .7 mL/mL 21749-0713-01 GOJO 30 ml — — Discontinued —
Instant Hand Sanitizer .7 mL/mLthis 62257-0061-47 ABC 473 ml — — FDA listed —
PDI Alcohol Prep Pad Sterile Large and Medium .7 mL/mL 10819-3914-01 Professional 200 packets — — FDA listed —
PDI Sani-Hands Instant Hand Sanitizing Wipes .7 mL/mL 10819-3916-01 Professional 100 packets — — FDA listed —
PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0702-08 GOJO 237 ml — — Discontinued —
PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel .7 mL/mL 21749-0717-08 GOJO 236 ml — — Discontinued —
Genuine First Aid Hand Sanitizer Ethyl Alcohol .7 mL/mL 50814-0060-01 GFA 60 ml — — FDA listed —
Genuine First Aid Hand Sanitizer with Cap Ethyl Alcohol .7 mL/mL 50814-0061-01 GFA 236 ml — — FDA listed —
Germ Attack Hand Sanitizer .7 mL/mL 66902-0443-02 Natural 60 ml — — FDA listed —
PURELL Advanced Hand Sanitizer be Vibrant .7 mL/mL 21749-0028-01 GOJO 30 ml — — FDA listed —
Genuine First Aid Hand Sanitizer Ethyl Alcohol .7 mL/mL 50814-0063-01 GFA 473 ml — — FDA listed —
North Woods Derma Gel Clear .7 mL/mL 53125-0801-04 Superior 3780 ml — — FDA listed —
Be Smart Get Prepared Hand Sanitizer .7 mL/mL 55550-0611-01 Total 1 ml — — FDA listed —
Alcohol Cleansing Wipe .7 mL/mL 83165-0001-00 Hubei 1 patch — — FDA listed —
PURELL Healthcare Advanced Hand Sanitizer Gel .7 mL/mL 21749-0716-01 GOJO 29 ml — — Discontinued —
Genuine First Aid Hand Sanitizer with Pump Ethyl Alcohol .7 mL/mL 50814-0062-01 GFA 236 ml — — FDA listed —
PURELL Advanced Hand Sanitizer be Blissful .7 mL/mL 21749-0029-01 GOJO 30 ml — — FDA listed —
Instant Hand Sanitizer .7 mL/mL 51824-0020-02 New 59 ml — — FDA listed —
PURELL Advanced Hand Sanitizer be Peaceful .7 mL/mL 21749-0027-01 GOJO 30 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Naturals Gel .7 mL/mL 21749-0625-01 GOJO 30 ml — — FDA listed —
Advanced Alcohol Gel Sanitizer .7 mL/mL 65601-0801-04 Betco 3780 ml — — FDA listed —
Tendersant Hand Sanitizer .7 mL/mL 69771-0007-01 Geri-Gentle 118 ml — — FDA listed —
Hand Sanitizer .7 mL/mL 70412-0194-15 Zhejiang 15 ml — — FDA listed —
Plus Brasept Alcocol Gel .7 mL/mL 83318-0605-14 NEWDROP 3785 ml — — Discontinued —
Germ Attack Hand Sanitizer .7 mL/mL 66902-0943-12 Natural 3785 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Green Certified Gel .7 mL/mL 21749-0708-08 GOJO 237 ml — — FDA listed —
Uline Hand Sanitizer .7 mL/mL 69790-0801-04 Uline 3780 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
Jul 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII WR1WPI7EW8
    A synthetic form of vitamin E used as an antioxidant. It prevents oils and fats in the medicine from breaking down and becoming rancid, helping keep the product stable during storage.
  • 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 809Y72KV36
    A synthetic polymer made from acrylic acid and crosslinked with allyl pentaerythritol. It's used as a thickening agent and gelling ingredient in creams, gels, and lotions to create the proper texture and help the medicine spread and stay on the skin.
  • UNII BR9JLI40NO
    A weak organic base used as a pH adjuster and neutralizing agent in liquid formulations. It helps maintain the proper acidity level so the medicine remains stable and effective in its container.
  • UNII BYR0546TOW
    DMDM hydantoin is a preservative chemical used to prevent the growth of bacteria and fungi in medicines. It helps keep the product safe and stable throughout its shelf life.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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.

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

The official label also stateswater, DMDM hydantoin, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis

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

LabelerABC Compounding Co., Inc.
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code62257
First marketedJul 2020
Product typeHuman Otc Drug
Portfolio15 products on file

More NDCs from ABC Compounding Co., Inc. labeler code 62257

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available

⏱️ Dosage and Administration 18 words ▾

Drug Facts Box OTC-Dosage & Administration Section wet hands thoroughly with product and allow to dry without wiping

⚠️ Warnings 16 words ▾

Drug Facts Box OTC-Warnings Section FLAMMABLE, keep away from fire and flames For external use only

🧪 Active Ingredient 10 words ▾

Drug Facts Box OTC-Active Ingredient Section Ethyl Alcohol 70% v/v

🧪 Inactive Ingredients 16 words ▾

Drug Facts Box OTC-Inactive Ingredient Section water, DMDM hydantoin, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis

🎯 Purpose 6 words ▾

Drug Facts Box OTC-Purpose Section Antiseptic

📄 When Using This Product 19 words ▾

Drug Facts Box OTC-When Using Section do not get into eyes if contact occurs, rinse eyes thoroughly with water

📄 Stop Use and Ask a Doctor If 10 words ▾

Drug Facts Box OTC-Stop Use Section irritation and redness develop

📄 Keep Out of Reach of Children 23 words ▾

Drug Facts Box OTC-Keep Out of Reach of Children Section if swallowed, get medical help or contact a Poison Control Center right away

📄 Package Label / Principal Display Panel 13 words ▾

Lynx 1605 Drug Facts and Label Lynx 1605 Instant Hand Sanitizer product label

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 ABC Compounding Co., 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 9 other package presentations of this same product, including 2.5 ml (62257-0061-21), 118 ml (62257-0061-24), 149 ml (62257-0061-28). 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?
ABC Compounding Co., 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.
← 62257-0012-06 · ABC 62257-0122-01 · ABC →
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.