Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Hand San ALCOHOL .7 mL/mL Liquid, 472 mL — NDC 59503-2605-1 (Billing 59503-2605-01)
by Rochester Midland Corporation · 472 mL in 1 BOTTLE, PLASTIC (59503-2605-1)
NDC 59503-2605-1 (billing 59503-2605-01) is a package of 472 mL of Hand San ALCOHOL .7 mL/mL Liquid from Rochester Midland Corporation, no longer marketed (first marketed Mar 2021), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 8 package sizes.
NDC 59503-2605-01
🏷️ FDA NDC (as labeled)
59503-2605-1
billing pads the package segment with a zero
This package
Contains472 mL
Pack sizes8 compare ↓
Main listing for product 59503-2605 · Also comes in:
946 ml 59503-2605-5
2500 ml 59503-2605-6
3785 ml 59503-2605-2
18900 ml 59503-2605-3
75600 ml 59503-2605-7
132500 ml 59503-2605-8
208200 ml 59503-2605-4
🗂️ FDA directory synced Oct 1, 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 →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
59503-2605-1
Product NDC
59503-2605
11-digit billing NDC
59503260501
UNII
3K9958V90M
Application #
M004
SPL Set ID
2d89982d-d1fd-4a98-8b44-c2ae3545be58
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2021-03-11
Route
TOPICAL
Dosage form
LIQUID
Substance
ALCOHOL
Quick answers for NDC 59503-2605-1
- 11-digit billing NDC: 59503260501
Why two NDCs?
The FDA registers this code as 59503-2605-1 — a 5-4-1 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 package segment → 59503-2605-01. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Sep 24, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
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...
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about ALCOHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 1, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 59503-2605-01 59503-2605-1 You're viewing this Main listing | 472 mL in 1 BOTTLE, PLASTIC (59503-2605-1) | 2021-03-11 | — | Discontinued by firm |
| 59503-2605-02 59503-2605-2 | 3785 mL in 1 BOTTLE, PLASTIC (59503-2605-2) | 2021-03-11 | — | Active |
| 59503-2605-03 59503-2605-3 | 18900 mL in 1 CONTAINER (59503-2605-3) | 2021-03-11 | — | Discontinued by firm |
| 59503-2605-04 59503-2605-4 | 208200 mL in 1 DRUM (59503-2605-4) | 2021-03-11 | — | Discontinued by firm |
| 59503-2605-05 59503-2605-5 | 946 mL in 1 BOTTLE, PLASTIC (59503-2605-5) | 2021-03-11 | — | Discontinued by firm |
| 59503-2605-06 59503-2605-6 | 2500 mL in 1 BOTTLE, PLASTIC (59503-2605-6) | 2021-03-11 | — | Discontinued by firm |
| 59503-2605-07 59503-2605-7 | 75600 mL in 1 DRUM (59503-2605-7) | 2021-03-11 | — | Active |
| 59503-2605-08 59503-2605-8 | 132500 mL in 1 DRUM (59503-2605-8) | 2021-03-11 | — | Active |
You're viewing the smallest of 8 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 59503-2605-01?
NDC 59503-2605-01 contains 472 mL — 472 ml in 1 bottle, plastic.
What is the difference between NDC 59503-2605-01 and NDC 59503-2605-05?
Both are Hand San ALCOHOL .7 mL/mL Liquid — the drug itself is identical. NDC 59503-2605-01 is the 472 mL package, while NDC 59503-2605-05 is the 946 ml package.
What NDC number is used to bill for this package of Hand San ALCOHOL .7 mL/mL Liquid?
Bill NDC 59503-2605-01 — the 11-digit billing format is 59503260501. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Recens Foam .7 mL/mL 75990-0968-07 | Certus | 700 ml | — | — | Discontinued | — |
| PURELL Advanced Hand Sanitizer Fragrance Free .7 mL/mL 21749-0532-01 | GOJO | 1.2 ml | — | — | FDA listed | — |
| Fast .7 mL/mL 62257-0658-08 | ABC | 1000 ml | — | — | Discontinued | — |
| PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 | GOJO | 450 ml | — | — | Discontinued | — |
| Lynx san a foam .7 mL/mL 62257-0007-10 | ABC | 1000 ml | — | — | FDA listed | — |
| EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 | TRIPLE | 1200 ml | — | — | FDA listed | — |
| PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0700-00 | GOJO | 1.2 ml | — | — | Discontinued | — |
| PURELL Advanced E3 Rated Instant Hand Sanitizer Foam .7 mL/mL 21749-0802-51 | GOJO | 550 ml | — | — | Discontinued | — |
| PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0806-51 | GOJO | 550 ml | — | — | Discontinued | — |
| PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0822-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Fragrance Free Foam .7 mL/mL 21749-0827-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Waterless Surgical Scrub .7 mL/mL 21749-0992-02 | GOJO | 59 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0826-53 | GOJO | 535 ml | — | — | FDA listed | — |
| Sani-Spritz .7 mL/mL 62257-0738-15 | ABC | 946 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Biobased Content .7 mL/mL 21749-0022-02 | GOJO | 60 ml | — | — | FDA listed | — |
| Hand San .7 mL/mLthis 59503-2605-01 | Rochester | 472 ml | — | — | Discontinued | — |
| PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 | GOJO | 515 ml | — | — | FDA listed | — |
| Germ Attack Hand Sanitizer .7 mL/mL 66902-0482-02 | Natural | 59 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Green Certified Foam .7 mL/mL 21749-0808-51 | GOJO | 550 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Gel .7 mL/mL 21749-0709-45 | GOJO | 450 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2021
On the market since
Mar 2021
📍
2026
Currently FDA-listed
5 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.
- FDA Orange Book · refreshed Sep 3, 2026
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 H3R47K3TBD
FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
-
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.
3 inactive ingredients listed in the exact product block matched to this NDC.
The official label also stateswater, propylene glycol, FD&C Blue #1
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerRochester Midland Corporation
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code59503
First marketedMar 2021
Product typeHuman Otc Drug
Portfolio3 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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 ▾
Drug Facts Box OTC-Indications and Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available
⏱️ Dosage and Administration ▾
Drug Facts Box OTC-Dosage & Administration Section Wet hands thoroughly with product and allow to dry without wiping
⚠️ Warnings ▾
Drug Facts Box OTC-Warnings Section Flammable, keep away from fire and flames For external use only
🧪 Active Ingredient ▾
Drug Facts Box OTC-Active Ingredient Section Ethyl Alcohol 70% v/v
🧪 Inactive Ingredients ▾
Drug Facts Box OTC-Inactive Ingredient Section water, propylene glycol, FD&C Blue #1
🎯 Purpose ▾
Drug Facts Box OTC-Purpose Section Antiseptic
📄 When Using This Product ▾
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 ▾
Drug Facts Box OTC-Stop Use Section irritation and redness develop
📄 Keep Out of Reach of Children ▾
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 ▾
Hand San 6150 Hand Aid 6150 Rochester Midland HandSan
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 ↗
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 Hand San (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.
About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.
Questions about this listing
Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 59503-2605-1, 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: 59503-2605-01, written without dashes as 59503260501. 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 59503-2605-01, the first segment (59503) is the labeler code FDA assigned to Rochester Midland Corporation; the middle segment (2605) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 7 other package presentations of this same product, including 946 ml (59503-2605-05), 2500 ml (59503-2605-06), 3785 ml (59503-2605-02). 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?
Rochester Midland Corporation 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.
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.