Lynx san a foam ALCOHOL .7 mL/mL Liquid, 1000 mL
by ABC Compounding Co., Inc. · 1000 mL in 1 CARTRIDGE (62257-007-10)
NDC 62257-0007-10
🏷️ FDA NDC (as labeled)
62257-007-10
billing pads the product segment with a zero
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)
62257-007-10
Product NDC
62257-007
11-digit billing NDC
62257000710
RxCUI
616805
UNII
3K9958V90M
UPC
0711808210774
Application #
M004
SPL Set ID
2b987ebc-c73b-edbd-e063-6394a90a1d2d
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2025-01-13
Route
TOPICAL
Dosage form
LIQUID
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 62257-007-10 — 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 → 62257-0007-10. 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
LabelerABC Compounding Co., Inc.
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code62257
First marketedJan 2025
Product typeHuman Otc Drug
Portfolio15 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 D76Z87928N
A synthetic polymer made by combining acrylate compounds with fluorinated components. It functions as a film-former and coating agent, helping create a protective layer on the tablet or capsule surface.
-
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, PEG-10 acrylate, perfluorohexylethyl acrylate copolymer, propylene glycol
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
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.
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 |
|---|---|---|---|---|---|---|
| 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 Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 | GOJO | 450 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 Gentle and Free Foam .7 mL/mL 21749-0826-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Fragrance Free Foam .7 mL/mL 21749-0827-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Moisturizing 2in1 Foam 70 mL/100mL 21749-0851-10 | GOJO | 295 ml | — | — | FDA listed | — |
| PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 | GOJO | 535 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam 70 mL/100mL 21749-0856-17 | GOJO | 515 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Naturals Foam 70 mL/100mL 21749-0875-10 | GOJO | 295 ml | — | — | FDA listed | — |
| Symmetry Foaming Hand Sanitizer Fragrance Free 70 mL/100mL 30805-0020-04 | Buckeye | 1200 ml | — | — | FDA listed | — |
| Symmetry Foaming Hand Sanitizer 70 mL/100mL 30805-0021-09 | Buckeye | 1000 ml | — | — | FDA listed | — |
| Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 70 mL/100mL 30805-0023-07 | Buckeye | 550 ml | — | — | FDA listed | — |
| I-70 Foaming .7 mL/mL 43097-0968-12 | People's | 1000 ml | — | — | FDA listed | — |
| ESC Protecting Foam Hand Sanitizer 76.9 mL/100mL 47593-0667-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab Retail Foaming Alcohol Hand Sanitizer 70 mL/100mL 47593-0685-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Kay Alcohol Foam Hand Sanitizer 70 mL/100mL 47593-0686-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Tork Hand Sanitizing Alcohol Foam 70 mL/100mL 49351-0301-01 | Essity | 1000 ml | — | — | FDA listed | — |
| Foaming Hand Sanitizer 70 mL/100mL 50021-0020-01 | Empack | 550 ml | — | — | FDA listed | — |
| MG FoamSan 70 .7 L/L 50241-0223-02 | Morgan | 3.785 l | — | — | FDA listed | — |
| EnMotion Foam Hand Sanitizer 70 mL/100mL 54622-0120-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| enMotion Foam High Frequency Use .7 mL/mL 54622-0121-01 | Georgia-Pacific | 2 bottles | — | — | FDA listed | — |
| Pacific Blue Ultra Foaming Fragrance Free 70 mg/mL 54622-0122-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| Pacific Blue Select Foam Hand Sanitizer, Fragrance Free, Dye Free 70 mL/100mL 54622-0311-01 | Georgia-Pacific | 24 bottles | — | — | FDA listed | — |
| enMotion Foam High Frequency Use 70 mL/100mL 54622-0486-01 | Georgia-Pacific | 1000 ml | — | — | FDA listed | — |
| Kleenex Ultra Moisturizing Hand Sanitizer 70 mL/100mL 55118-0530-10 | Kimberly-Clark | 1000 ml | — | — | Discontinued | — |
| Kleenex Reveal Moisturizing Foam Hand Sanitizer 70 mL/100mL 55118-0531-10 | Kimberly-Clark | 6 bottles | — | — | Discontinued | — |
| Lynx san a foam .7 mL/mLthis 62257-0007-10 | ABC | 1000 ml | — | — | FDA listed | — |
| Fast .7 mL/mL 62257-0658-08 | ABC | 1000 ml | — | — | Discontinued | — |
| Dermacen Foaming Instant Hand Sanitizer With Aloe 70 mL/100mL 62654-0149-13 | Central | 1000 ml | — | — | FDA listed | — |
| Saniclean 70 g/100mL 63900-0150-02 | Simoniz | 1000 ml | — | — | FDA listed | — |
| Foaming Instant Hand Sanitizer with Aloe 70 g/100g 68599-5205-01 | MCKESSON | 251 g | — | — | FDA listed | — |
| Hand Sanitizer 70 mL/100mL 69790-0456-44 | Uline | 532 ml | — | — | FDA listed | — |
| EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 | TRIPLE | 1200 ml | — | — | FDA listed | — |
| Hand Sanitizer 70 mL/100mL 71897-0465-86 | Veritiv | 1000 ml | — | — | FDA listed | — |
| Clean Revolution Foaming Hand Sanitizer Refill Supply Container - Gentle and Aloe Enriched - ELIMINATES 99.9% Germs - 70% Ethanol - Ready To Use 70 mL/100mL 74810-0725-00 | Replenish | 3785 ml | — | — | FDA listed | — |
| Recens Foam .7 mL/mL 75990-0968-07 | Certus | 700 ml | — | — | Discontinued | — |
| Hand Sanitizer 70 mL/100mL 76370-0003-01 | Tazza | 10000 ml | — | — | Discontinued | — |
| Hand Sanitizer 70 mL/100mL 76370-0005-02 | Tazza | 3785 ml | — | — | Discontinued | — |
| Tazza 70% Alcohol-Based Hand Sanitizing Foam 70 L/100L 76370-0033-00 | Tazza | 3.785 l | — | — | FDA listed | — |
| Hand Sanitizer Foam 70 mL/100mL 77955-0002-02 | Custom | 1000 ml | — | — | FDA listed | — |
| Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0101-12 | Archer | 1000 ml | — | — | FDA listed | — |
| Black Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0102-12 | Archer | 1000 ml | — | — | FDA listed | — |
| KleenLine Essentials Foaming Hand Sanitizer .7 mL/mL 79258-0802-29 | Brady | 1000 ml | — | — | FDA listed | — |
| MyHealth Advanced Hand Sanitizer 70 mL/100mL 80661-0002-01 | Aeroflex | 150 ml | — | — | FDA listed | — |
| Novo Foaming Instant Hand Sanitizer .7 mL/mL 81551-0802-04 | Noble | 3785 ml | — | — | FDA listed | — |
| Foaming Hand Alcohol Foam 70 mL/100mL 83019-0102-11 | Draco | 1000 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Fragrance Free .7 mL/mL 21749-0532-01 | GOJO | 1.2 ml | — | — | FDA listed | — |
| PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0700-00 | GOJO | 1.2 ml | — | — | Discontinued | — |
| PURELL Waterless Surgical Scrub .7 mL/mL 21749-0992-02 | GOJO | 59 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/mL 59503-2605-01 | Rochester | 472 ml | — | — | Discontinued | — |
| 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.
⏳ Availability & generic status
🏛️
2025
On the market since
Jan 2025
📍
2026
Currently FDA-listed
1 year 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 |
|---|---|---|---|
| 62257-0007-10 You're viewing this | 1000 mL in 1 CARTRIDGE (62257-007-10) | 2025-01-13 | Active |
🧭 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 62257-007-10, 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: 62257-0007-10, written without dashes as 62257000710. 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 62257-0007-10, the first segment (62257) is the labeler code FDA assigned to ABC Compounding Co., Inc.; the middle segment (0007) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (10) 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 ABC Compounding Co., Inc.. Listing status can change — the directory data on this page refreshes weekly.
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.
📄 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
🎯 Indications and Usage ▾
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 ▾
Drug Facts Box OTC-Dosage & Administration Section apply to hands and rub lightly until dry without wiping or rinsing
⚠️ 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, PEG-10 acrylate, perfluorohexylethyl acrylate copolymer, propylene glycol
🎯 Purpose ▾
Drug Facts Box OTC-Purpose Section Antiseptic
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.