ALCOHOL 62 mL/100mL Gel, 44 mL
by Scribe Opco, Inc. · 44 mL in 1 BOTTLE (52675-400-44)
NDC 52675-0400-44
🏷️ FDA NDC (as labeled)
52675-400-44
billing pads the product segment with a zero
This package
Contains44 mL
Pack sizes3 compare ↓
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)
52675-400-44
Product NDC
52675-400
11-digit billing NDC
52675040044
SPL Set ID
1d7de948-fd92-6a8b-e063-6294a90a4c96
DEA schedule
Non-controlled
Marketing category
DRUG FOR FURTHER PROCESSING
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2010-11-05
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 52675-400-44 — 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 → 52675-0400-44. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.
🏭 Manufacturer & labeler
LabelerScribe Opco, Inc.
Labeler code52675
First marketedNov 2010
Product typeDrug For Further Processing
Portfolio6 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.
We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.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 g | 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 |
|---|---|---|---|---|---|---|
| QUR Lavender essential oil hand sanitizer 62 mL/100mL 81761-0111-01 | Qur, | 30 ml | — | — | FDA listed | — |
| QUR Vanilla essential oil hand sanitizer 62 mL/100mL 81761-0112-01 | Qur, | 30 ml | — | — | FDA listed | — |
| PURELL Cottony Soft Hand Sanitizing Wipe 62 mL/100mL 21749-0364-76 | GOJO | 1 pouch | — | — | FDA listed | — |
| Strawberry Pound Cake SCENTED HAND SANITIZER 62 mL/100mL 85588-0203-01 | MELON | 29 ml | — | — | FDA listed | — |
| Hand Sanitizer 62 mL/100mL 77955-0001-02 | Custom | 1000 ml | — | — | FDA listed | — |
| Hand Sanitizer 62 mL/100mL 83986-0652-04 | UpLift | 750 ml | — | — | FDA listed | — |
| Hand Sanitizer Lemon Scented 62 mL/100mL 87614-0002-01 | Taizhou | 60 ml | — | — | FDA listed | — |
| PURELL Hand Sanitizing Wipe 62 mL/100mL 21749-0363-76 | GOJO | 1 pouch | — | — | FDA listed | — |
| Instant Hand Antiseptic 62 mL/100mL 59448-0001-02 | ASP | 53 ml | — | — | FDA listed | — |
| Instant Hand Antiseptic 62 mL/100mL 59448-0004-01 | ASP | 53 ml | — | — | FDA listed | — |
| antibacterial hand sanitizer gel 01 62 mL/100mL 82953-0022-01 | Cosmuses | 15 ml | — | — | FDA listed | — |
| Vanilla Sugar SCENTED HAND SANITIZER 62 mL/100mL 85588-0202-01 | MELON | 29 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 52675-0230-30 | Scribe | 30 ml | — | — | FDA listed | — |
| PURELL Hand Sanitizing Wipes Alcohol Formula 62 mL/100mL 21749-0367-36 | GOJO | 101 ml | — | — | FDA listed | — |
| EO Hand Sanitizer Wipes Lavender 62 mL/100mL 54748-0502-01 | EO | 3 ml | — | — | FDA listed | — |
| Sanitaxe 27 Oz Instant Hand Sanitizer With Aloe Vera 62 mL/100mL 72197-0032-27 | American | 800 ml | — | — | FDA listed | — |
| Pink Pineapple SCENTED HAND SANITIZER 62 mL/100mL 85588-0201-01 | MELON | 29 ml | — | — | FDA listed | — |
| Genuine First Aid Hand Sanitizer 62 mL/100mL 50814-0078-01 | GFA | 1.03 ml | — | — | FDA listed | — |
| EO HAND SANITIZER Unscented 62 mL/100mL 54748-0203-07 | EO | 946 ml | — | — | FDA listed | — |
| Hand Sanitizer 62 mL/100mL 73288-0008-01 | NINGBO | 500 packets | — | — | FDA listed | — |
| Servo-Stat 62 mL/100mL 76378-0015-01 | Enzyme | 118 ml | — | — | FDA listed | — |
| Hand Sanitizer with Aloe 62 mL/100mL 83986-0826-16 | UpLift | 59 ml | — | — | FDA listed | — |
| EOCENE Dr. HANITIZER 62 mL/100mL 73466-0006-01 | MISOCOS | 100 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mLthis 52675-0400-44 | Scribe | 44 ml | — | — | FDA listed | — |
| health beyond HAND SANITIZER 62 mL/100mL 43473-0075-01 | Nantong | 500 packets | — | — | FDA listed | — |
| Sanifoam Hand Sanitizer 62 mL/100mL 50536-0078-01 | AMERICAN | 3785 ml | — | — | FDA listed | — |
| Hand Sanitizer Rebel Cherry 62 mL/100mL 76891-0136-11 | SCENT | 29 ml | — | — | FDA listed | — |
| antibacterial hand sanitizer gel 01 62 mL/100mL 82953-0016-01 | Cosmuses | 15 ml | — | — | FDA listed | — |
| Alcohol 62 mL/100mL 52675-0300-01 | Scribe | 29 ml | — | — | FDA listed | — |
| Hand Sanitizer Coconut Breeze 62 mL/100mL 76891-0135-11 | SCENT | 29 ml | — | — | FDA listed | — |
| Mada 62 mL/100mL 11928-0004-04 | Mada | 118 ml | — | — | FDA listed | — |
| Aosi Healthcare Hand Sanitizer 62 mL/100mL 43473-0056-01 | Nantong | 9 ml | — | — | FDA listed | — |
| EO HAND SANITIZER Lavender 62 mL/100mL 54748-0201-05 | EO | 59 ml | — | — | FDA listed | — |
| Hand Sanitizing with Lavender Oil 62 mL/100mL 59088-0413-06 | PureTek | 1 bottle | — | — | FDA listed | — |
| Pharmacys Prescription 8Oz Hand Sanitizer 62 mL/100mL 72197-0011-08 | American | 237 ml | — | — | FDA listed | — |
| Sweet Coconut SCENTED HAND SANITIZER 62 mL/100mL 85588-0204-01 | MELON | 29 ml | — | — | FDA listed | — |
| Prevent Hand Sanitizer 62 mL/100mL 50536-0077-12 | AMERICAN | 3785 ml | — | — | FDA listed | — |
| Instant Hand Antiseptic 62 mL/100mL 59448-0008-01 | ASP | 53 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
🏛️
2010
On the market since
Nov 2010
📍
2026
Currently FDA-listed
16 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 Alcohol — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 47%
Female · 52%
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 |
|---|---|---|---|
| 52675-0400-30 | 29.6 mL in 1 BOTTLE (52675-400-30) | — | Active |
| 52675-0400-44 You're viewing this | 44 mL in 1 BOTTLE (52675-400-44) | — | Active |
| 52675-0400-74 | 73.9 mL in 1 BOTTLE (52675-400-74) | — | Active |
Pack size FAQ
What quantity is in NDC 52675-0400-44?
NDC 52675-0400-44 contains 44 mL — 44 ml in 1 bottle.
What is the difference between NDC 52675-0400-44 and NDC 52675-0400-30?
Both are ALCOHOL 62 mL/100mL Gel — the drug itself is identical. NDC 52675-0400-44 is the 44 mL package, while NDC 52675-0400-30 is the 29.6 ml package.
What NDC number is used to bill for this package of ALCOHOL 62 mL/100mL Gel?
Bill NDC 52675-0400-44 — the 11-digit billing format is 52675040044. 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
Listed for further processing / repackaging
What "drug for further processing" means
FDA lists this package under the "drug for further processing" marketing category: Scribe Opco, Inc. supplies it to other companies for further processing or repackaging (blister cards that are later repackaged or co-packaged are a common example). The units themselves are a finished dosage form — which is why pricing or Medicaid data can still appear — but this exact package code may not be the presentation a retail pharmacy dispenses.
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 | — Not published for this NDC No photo available yet for this listing. |
| Inactive ingredients (structured) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 "Drug For Further Processing". 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 52675-400-44, 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: 52675-0400-44, written without dashes as 52675040044. 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 52675-0400-44, the first segment (52675) is the labeler code FDA assigned to Scribe Opco, Inc.; the middle segment (0400) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (44) 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 Scribe Opco, 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 29.6 ml (52675-0400-30), 73.9 ml (52675-0400-74). 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?
Scribe Opco, 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.
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.
📄 Full FDA label FDA SPL
The complete FDA label for this product, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 FDA label ▾
No FDA label is on file for this product yet. Labels load from openFDA / DailyMed and refresh weekly.
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.