Lavender Hand Sanitizer Wipes Ethanol 65 mL/100mL Cloth, 234 mL
by Whole Foods Market, Inc. · 234 mL in 1 CANISTER (42681-6809-3)
NDC 42681-6809-03
🏷️ FDA NDC (as labeled)
42681-6809-3
billing pads the package segment with a zero
This package
Contains234 mL
Pack sizes2 compare ↓
Also comes in:
40 canisters 42681-6809-01
OTC
On market
Non-controlled
🗂️ Data synced Sep 17, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Ethanol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 22, 2026 — Microbial contamination of sterile products (Zep Inc) · FDA recall D-0586-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
🆔 Identity & classification
FDA NDC (as labeled)
42681-6809-3
Product NDC
42681-6809
11-digit billing NDC
42681680903
RxCUI
884787
UNII
3K9958V90M
Application #
505G(a)(3)
SPL Set ID
664dc461-4be0-49e0-bf2b-4a3ce0606cd8
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2021-05-05
Route
TOPICAL
Dosage form
CLOTH
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 42681-6809-3 — 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 → 42681-6809-03. 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
LabelerWhole Foods Market, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code42681
First marketedMay 2021
Product typeHuman Otc Drug
Portfolio46 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
Some supplements/herbs that may interact with Ethanol — tap one for details:
4
Nutrient depletion considerations
Ethanol may be associated with lower levels of 4 nutrients — worth a chat with your pharmacist, not a cause for alarm.
VITAMIN C
Insignificant Depletion
FOLIC ACID
Moderate Depletion
GLUTATHIONE
Insufficient Evidence
ZEAXANTHIN
Insufficient Evidence
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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 Ethanol?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
white
ShapeRectangle
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 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 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 TRW2FUF47H
A plant-derived powder from marshmallow root used as a binder and thickener in medicines. It helps hold ingredients together and can soothe irritated surfaces in throat lozenges and syrups.
-
UNII FGL3685T2X
Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
-
UNII YY7C30VXJT
A natural plant extract from cucumber that adds flavor and freshness to medicines. It may also serve as a moisturizing agent or mild preservative in topical or oral formulations.
-
UNII PDC6A3C0OX
Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
-
UNII ND2M416302
Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
-
UNII ZBP1YXW0H8
A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
-
UNII Z6J799EAJK
Oat is a cereal grain used in medicines as a filler and binder. It helps give the medication its shape and structure while adding bulk to the formulation.
8 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, Isopropyl Alcohol, Glycerin, Lavandula Angustifolia (Lavender) Oil, Organic Aloe Barbadensis Leaf Extract, Organic Althaea Officinalis Root Extract, Organic Avena Sativa (Oats) Extract, Organic Camellia Sinensis (White Tea) Leaf Extract, Organic Chamomilla Recutita (Matricaria) Flower Extract, Organic Cucumis Sativus (Cucumber) Fruit Extract
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 each | 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.
Try another pack size:
40 canisters
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 |
|---|---|---|---|---|---|---|
| 365 Spiced Balsam Hand Sanitizer Wipes 2.55 mL 42681-0041-01 | Whole | 10 cloths | — | — | FDA listed | — |
| 365 Winterberry Saffron Hand Sanitizer Wipes 2.55 mL 42681-0042-01 | Whole | 10 cloths | — | — | FDA listed | — |
| 365 Spiced Citrus Hand Sanitizer Wipes 2.55 mL 42681-0043-01 | Whole | 10 cloths | — | — | FDA listed | — |
| Lavender Hand Sanitizer Wipes 65 mL/100mL 42681-6808-01 | Whole | 10 pouches | — | — | Discontinued | — |
| Lavender Hand Sanitizer Wipes 65 mL/100mLthis 42681-6809-03 | Whole | 234 ml | — | — | FDA listed | — |
| Lavender Hand Sanitizing Wipes 65 mL/100mL 42681-6810-01 | Whole | 210 canisters | — | — | Discontinued | — |
| Sanitizing Wipes Fragrance Free 65 mL/100mL 69366-0316-24 | The | 50 patches | — | — | FDA listed | — |
| Sanitizing wipes with aloe Grapefruit Grove 65 mL/100mL 69366-0317-24 | The | 50 patches | — | — | Discontinued | — |
| Sanitizing Wipes Lavender 65 mL/100mL 69366-0319-24 | The | 50 ml | — | — | FDA listed | — |
| Sanitizing Wipes Grapefruit 65 mL/100mL 69366-0320-24 | The | 50 ml | — | — | FDA listed | — |
| Nourishing Sanitizing Hand Wipes Lavendula 65 mL/100mL 73898-0100-01 | Noshinku | 58.79 ml | — | — | FDA listed | — |
| Nourishing Sanitizing Hand Wipes Eucalyptus 65 mL/100mL 73898-0101-01 | Noshinku | 58.79 ml | — | — | FDA listed | — |
| Nourishing Sanitizing Hand Wipes Bergamot 65 mL/100mL 73898-0102-01 | Noshinku | 58.79 ml | — | — | FDA listed | — |
| Hand Sanitizing Wipe 65 mL/100mL 81339-0100-24 | NeatGoods | 24 packets | — | — | FDA listed | — |
| Hand Sanitizer 65 mL/100mL 81339-0101-24 | NeatGoods | 1 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
🏛️
2021
On the market since
May 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.
🔬 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 Lavender Hand Sanitizer Wipes (this brand).
Top reported reactions
Reporter sex
Male · 53%
Female · 47%
Unknown · 1%
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 |
|---|---|---|---|
| 42681-6809-01 | 40 CANISTER in 1 CANISTER (42681-6809-1) / 195 mL in 1 CANISTER | 2018-02-01 | Inactivated by FDA |
| 42681-6809-03 You're viewing this | 234 mL in 1 CANISTER (42681-6809-3) | 2021-05-05 | Active |
Pack size FAQ
What quantity is in NDC 42681-6809-03?
NDC 42681-6809-03 contains 234 mL — 234 ml in 1 canister.
What NDC number is used to bill for this package of Lavender Hand Sanitizer Wipes Ethanol 65 mL/100mL Cloth?
Bill NDC 42681-6809-03 — the 11-digit billing format is 42681680903. 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) | ✓ 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 42681-6809-3, 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: 42681-6809-03, written without dashes as 42681680903. 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 42681-6809-03, the first segment (42681) is the labeler code FDA assigned to Whole Foods Market, Inc.; the middle segment (6809) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Whole Foods Market, 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 1 other package presentation of this same product, including 40 canisters (42681-6809-01). 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?
Whole Foods Market, 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 ▾
Uses for hand sanitizing to decrease bacteria on skin when water and soap are not available. recommended for repeated use.
⏱️ Dosage and Administration ▾
Directions remove wipe wet hands thoroughly with wipe and allow hands to dry without wiping
⚠️ Warnings ▾
Warnings For external use only. Flammable: keep away from fire or flame. When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water. Stop use and contact a doctor if irritation or redness persists for more than 72 hours.
🧪 Active Ingredient ▾
Active Ingredient Ethyl Alcohol 65% V/V
🧪 Inactive Ingredients ▾
Inactive ingredients Water, Isopropyl Alcohol, Glycerin, Lavandula Angustifolia (Lavender) Oil, Organic Aloe Barbadensis Leaf Extract, Organic Althaea Officinalis Root Extract, Organic Avena Sativa (Oats) Extract, Organic Camellia Sinensis (White Tea) Leaf Extract, Organic Chamomilla Recutita (Matricaria) Flower Extract, Organic Cucumis Sativus (Cucumber) Fruit Extract
🎯 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.