Avant Original - Fragrance Free Alcohol 60 mL/100mL Gel, 1920 mL
by B4 Soap LLC · 1920 mL in 1 BOTTLE, PLASTIC (68306-106-06)
NDC 68306-0106-06
🏷️ FDA NDC (as labeled)
68306-106-06
billing pads the product segment with a zero
This package
Contains1920 mL
Pack sizes11 compare ↓
Also comes in:
59 ml 68306-0106-11
60 ml 68306-0106-04
82.5 ml 68306-0106-01
120 ml 68306-0106-05
251 ml 68306-0106-12
500 ml 68306-0106-02
1000 ml 68306-0106-03
1000 ml 68306-0106-10
3785 ml 68306-0106-08
208198 ml 68306-0106-09
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)
68306-106-06
Product NDC
68306-106
11-digit billing NDC
68306010606
RxCUI
581658
UNII
3K9958V90M
Application #
505G(a)(3)
SPL Set ID
35a2d0ba-9209-4d70-b3b4-537225f83c84
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2010-05-15
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 68306-106-06 — 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 → 68306-0106-06. 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
LabelerB4 Soap LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code68306
First marketedMay 2010
Product typeHuman Otc Drug
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.
Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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 |
|---|---|---|---|---|---|---|
| Isagel 600 mL/1000mL 11701-0025-45 | Coloplast | 800 ml | — | — | Discontinued | — |
| Ecolab 60 mL/100mL 47593-0507-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab Facilipro 60 mL/100mL 47593-0508-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Ecolab Clear 60 mL/100mL 47593-0638-41 | Ecolab | 750 ml | — | — | Discontinued | — |
| SSDC Gel Hand Sanitizer 60 mL/100mL 47593-0664-70 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Covex Antibacterial Hand Sanitizer, COOL BREEZE .6 mL/mL 51209-0012-00 | DALAN | 236 ml | — | — | FDA listed | — |
| Covex Antibacterial Hand Sanitizer, FRESH ALOE .6 mL/mL 51209-0013-00 | DALAN | 236 ml | — | — | FDA listed | — |
| Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer 600 mL/L 51801-0437-08 | Nomax, | 237 l | — | — | FDA listed | — |
| SunDrops 75 .6 mL/mL 63621-0356-14 | Sunburst | 3785 ml | — | — | FDA listed | — |
| Aire-Master Hand Sanitizer 600 mL/L 65585-0358-01 | Whisk | 473 l | — | — | FDA listed | — |
| Sani-Sure 600 mL/L 65585-0359-01 | Whisk | 237 l | — | — | FDA listed | — |
| WhiskCare 375 600 mL/L 65585-0375-01 | Whisk | 8 l | — | — | Discontinued | — |
| WhiskCare 375 Fragrance Free 600 mL/L 65585-0378-01 | Whisk | 8 l | — | — | FDA listed | — |
| Pacific Breeze Instant Hand Sanitizer Gel 600 mL/L 65585-0380-01 | Whisk | 1 l | — | — | FDA listed | — |
| D-Germ 600 mL/L 65585-0498-01 | Whisk | 118 l | — | — | FDA listed | — |
| Algonquin HanSan 600 mL/L 65585-0522-02 | Whisk | 237 l | — | — | FDA listed | — |
| Aire-Master Waterless Hand Sanitizer 600 mL/L 65585-0525-01 | Whisk | 8 l | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2074-01 | Raining | 44 ml | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2075-01 | Raining | 30 ml | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2076-01 | Raining | 59 ml | — | — | FDA listed | — |
| Vindicator Instant Hand Sanitizer 600 mL/1000mL 66608-0515-05 | Kimball | 3785 ml | — | — | Discontinued | — |
| Natural Extensions Fragrance- Free Instant Hand Sanitizer 60 mL/100mL 66975-0101-02 | Benco | 251 ml | — | — | FDA listed | — |
| Applause 3 g/5g 67858-0693-02 | QuestSpecialty | 24 bottles | — | — | FDA listed | — |
| Avant Original - Fragrance Free 60 mL/100mLthis 68306-0106-06 | B4 | 1920 ml | — | — | FDA listed | — |
| Zogics Instant Hand Sanitizer Hydrating Gel 60 mL/100mL 72202-0026-01 | Zogics, | 1000 ml | — | — | FDA listed | — |
| palm party 60 mL/100mL 87322-1614-01 | Dongyang | 30 ml | — | — | FDA listed | — |
| Clean and Go 600 mL/1000mL 87377-0001-01 | Satellite | 800 ml | — | — | Discontinued | — |
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
May 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 68306-0106-01 | 82.5 mL in 1 BOTTLE, DISPENSING (68306-106-01) | 2010-05-15 | Discontinued by firm |
| 68306-0106-02 | 500 mL in 1 BOTTLE, PUMP (68306-106-02) | 2010-05-15 | Active |
| 68306-0106-03 | 1000 mL in 1 POUCH (68306-106-03) | 2010-05-15 | Active |
| 68306-0106-04 | 60 mL in 1 BOTTLE, DISPENSING (68306-106-04) | 2010-05-15 | Active |
| 68306-0106-05 | 120 mL in 1 BOTTLE, DISPENSING (68306-106-05) | 2010-05-15 | Discontinued by firm |
| 68306-0106-06 You're viewing this | 1920 mL in 1 BOTTLE, PLASTIC (68306-106-06) | 2010-05-15 | Active |
| 68306-0106-08 | 3785 mL in 1 JUG (68306-106-08) | 2010-05-15 | Active |
| 68306-0106-10 | 1000 mL in 1 CARTRIDGE (68306-106-10) | 2012-05-01 | Active |
| 68306-0106-11 | 59 mL in 1 BOTTLE, PLASTIC (68306-106-11) | 2020-05-01 | Active |
| 68306-0106-12 | 251 mL in 1 BOTTLE, PUMP (68306-106-12) | 2010-05-15 | Active |
| 68306-0106-09 | 208198 mL in 1 DRUM (68306-106-09) | 2023-04-04 | Active |
Pack size FAQ
What quantity is in NDC 68306-0106-06?
NDC 68306-0106-06 contains 1920 mL — 1920 ml in 1 bottle, plastic.
What is the difference between NDC 68306-0106-06 and NDC 68306-0106-11?
Both are Avant Original - Fragrance Free Alcohol 60 mL/100mL Gel — the drug itself is identical. NDC 68306-0106-06 is the 1920 mL package, while NDC 68306-0106-11 is the 59 ml package.
What NDC number is used to bill for this package of Avant Original - Fragrance Free Alcohol 60 mL/100mL Gel?
Bill NDC 68306-0106-06 — the 11-digit billing format is 68306010606. 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) | — 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 "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 68306-106-06, 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: 68306-0106-06, written without dashes as 68306010606. 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 68306-0106-06, the first segment (68306) is the labeler code FDA assigned to B4 Soap LLC; the middle segment (0106) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (06) 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 B4 Soap LLC. 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 10 other package presentations of this same product, including 59 ml (68306-0106-11), 60 ml (68306-0106-04), 82.5 ml (68306-0106-01). 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?
B4 Soap LLC 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 ▾
Uses Hand sanitizer to help reduce bacteria on the skin Recommended for repeated use
⏱️ Dosage and Administration ▾
Directions Dispense an adequate amount in your palm to cover all surfaces of hands completely. Rub hands together until dry. Supervise children in the use of this product.
⚠️ Warnings ▾
Warnings For external use only . Flammable, keep away from fire or flame . When using this product do not use in or near eyes. In case of eye contact, flush thoroughly with water. Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active Ingredient Ethanol 60%
🧪 Inactive Ingredients ▾
Inactive Ingredients Water, Propylene Glycol, Triethanolamine, Carbomer, Glycerin
🎯 Purpose ▾
Purpose Antimicrobial
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.