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Sanitizing Wipes Fragrance Free Alcohol 65 mL/100mL Cloth, 50 patches — NDC 69366-0316-24 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Sanitizing Wipes Fragrance Free Alcohol 65 mL/100mL Cloth, 50 patches — NDC 69366-316-24 (Billing 69366-0316-24)

by The Honest Company · 50 PATCH in 1 POUCH / 4.32 mL in 1 PATCH

This is a package of 50 patches of Sanitizing Wipes Fragrance Free Alcohol 65 mL/100mL Cloth from The Honest Company, marketed since Feb 2023 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 69366-0316-24
🏷️ FDA NDC (as labeled) 69366-316-24 billing pads the product segment with a zero
This package
Contains50 patches Pack sizes2 compare ↓
Main listing for product 69366-316 · Also comes in: 150 patches 69366-316-25
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 69366-316-24 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69366 labeler · 316 product · 24 package
Package marketed since
Feb 1, 2023
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6936631624 9
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69366-316-24
Product NDC 69366-316
11-digit billing NDC 69366031624
RxCUI 884787
UNII 3K9958V90M
Application # M003
SPL Set ID 0ce3e7ee-aa50-16bc-e063-6294a90a527d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-02-01
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 884787
Why two NDCs? The FDA registers this code as 69366-316-24 — 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 → 69366-0316-24. 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.

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...
📖 Read our full Alcohol guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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 systemPer eachPer 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: 150 patches
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
69366-0316-24 You're viewing this Main listing 50 PATCH in 1 POUCH / 4.32 mL in 1 PATCH 2023-02-01 — Active
69366-0316-25 69366-316-25 150 PATCH in 1 POUCH / 4.32 mL in 1 PATCH 2023-02-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 50 patches — 50 patch in 1 pouch / 4.32 ml in 1 patch.
How does this package differ from NDC 69366-0316-25?
Both are Sanitizing Wipes Fragrance Free Alcohol 65 mL/100mL Cloth — the drug itself is identical. This page's package is the 50 patches one, while NDC 69366-0316-25 is the 150 patches package.
What NDC number is used to bill for this package of Sanitizing Wipes Fragrance Free Alcohol 65 mL/100mL Cloth?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice 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/100mL 42681-6809-01 Whole 40 canisters — — Discontinued —
Lavender Hand Sanitizing Wipes 65 mL/100mL 42681-6810-01 Whole 210 canisters — — Discontinued —
Sanitizing Wipes Fragrance Free 65 mL/100mLthis 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 —
Kills Hand Sanitizer 65 mL/100mL 58466-0105-08 Dermazone 236 ml — — FDA listed —
Hand Sanitizer 65 mL/100mL 56194-0503-01 Giant 30 ml — — FDA listed —
Berris And Creamy Scented Hand Sanitizer 65 mL/100mL 56136-0445-01 Ganzhou 29 ml — — FDA listed —
Strawberry Shortcake Scented Hand Sanitizer 65 mL/100mL 56136-0446-01 Ganzhou 29 ml — — FDA listed —
Hand sanitizer 29ml 01 65 mL/100mL 54860-0405-01 Shenzhen 29 ml — — FDA listed —
Mango Sorbet Scented Hand Sanitizer 65 mL/100mL 56136-0443-01 Ganzhou 29 ml — — FDA listed —
Coconut Vanilla Scented Hand Sanitizer 65 mL/100mL 56136-0444-01 Ganzhou 29 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

🏛️
2023
On the market since
Feb 2023
📍
2026
Currently FDA-listed
3 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.

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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 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 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 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 statesAloe Barbadensis Leaf Extract, Glycerin, Water

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.

Manufacturer & labeler

LabelerThe Honest Company
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code69366
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from The Honest Company labeler code 69366

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 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 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses Helps reduce bacteria on the skin Recommended for repeated use

⏱️ Dosage and Administration 26 words ▾

Directions Wipe hands thoroughly with product when there's no soap and water around. Discard after use, please don't flush For children under 6, use adult supervision

⚠️ Warnings 20 words ▾

For external use only. Flammable, Keep away from the fire, sparks, and sources of ignition Do not store above 104F/40C

🧪 Active Ingredient 3 words ▾

Ethyl Alcohol 65%

🧪 Inactive Ingredients 6 words ▾

Aloe Barbadensis Leaf Extract, Glycerin, Water

🎯 Purpose 1 words ▾

Antiseptic

📄 When Using This Product 13 words ▾

Keep out of eyes Incase of contact with eyes, flush thoroughly with water

📄 Stop Use and Ask a Doctor If 18 words ▾

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours

📄 Keep Out of Reach of Children 12 words ▾

if swallowed, get medical help or contact a Poison Control Center immediately

📄 Other Information 19 words ▾

Other Information Not for use as a baby wipe Do not use in genital area or on damaged skin

📄 Package Label / Principal Display Panel 11 words ▾

Fragrance Free Sanitizing Wipe 50ct NDC 69366-316-24 FF Sanitizing Wipe 50ct

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 The Honest Company. 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 150 patches (69366-0316-25). 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?
The Honest Company 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.
← 69366-0312-04 · The 69366-0317-24 · The →
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.