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PDI Sani Hands Instant Hand Sanitizing Wipes .7 mL/mL Cloth, 20 applicators — NDC 10819-3918-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

PDI Sani Hands Instant Hand Sanitizing Wipes .7 mL/mL Cloth, 20 applicators — NDC 10819-3918-1 (Billing 10819-3918-01)

by Professional Disposables International Inc · 20 APPLICATOR in 1 CELLO PACK / 4.15 mL in 1 APPLICATOR

This is a package of 20 applicators of PDI Sani Hands Instant Hand Sanitizing Wipes .7 mL/mL Cloth from Professional Disposables International Inc, marketed since Apr 2016 and currently FDA-listed. It is this product's only package size.

NDC 10819-3918-01
🏷️ FDA NDC (as labeled) 10819-3918-1 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 10819-3918-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
10819 labeler · 3918 product · 1 package
Package marketed since
Apr 1, 2016
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 1081939181 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 10819-3918-1
Product NDC 10819-3918
11-digit billing NDC 10819391801
RxCUI 1489307
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 2fff2a3d-5ea9-346e-e054-00144ff8d46c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-04-01
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1489307
Why two NDCs? The FDA registers this code as 10819-3918-1 — 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 → 10819-3918-01. 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.
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
10819-3918-01 You're viewing this Main listing 20 APPLICATOR in 1 CELLO PACK / 4.15 mL in 1 APPLICATOR 2016-04-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PDI Sani-Hands Instant Hand Sanitizing Wipes .7 mL/mL 10819-3916-01 Professional 100 packets — — FDA listed —
PDI Sani Hands .7 mL/mLthis 10819-3918-01 Professional 20 applicators — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6006-01 Professional 3.23 ml — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6007-01 Professional 484 ml — — FDA listed —
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6008-01 Professional 805.44 ml — — FDA listed —
Signature Select Instant Hand Sanitizer Wipes with Aloe Vera 70 mL/100mL 21130-0068-01 Living 24 patches — — FDA listed —
Jianerkang Sanitizing Wipe .7 mL/mL 34645-0003-01 Jianerkang 1 patch — — FDA listed —
Instant Hand Sanitizer STERILE 70 Ethyl Alcohol .7 mL/mL 34645-0007-01 Jianerkang 1 patch — — FDA listed —
microdot Hand Sanitizing Wipe 70 mL/100mL 52422-0622-06 Cambridge 563.91 ml — — FDA listed —
Spectrum Hand Sanitizer Wipes 70 mL/100mL 53329-0840-32 Medline 20 applicators — — FDA listed —
Procure Products Hand Sanitizing Wipes 70 mL/100mL 55681-0135-02 TWIN 135 patches — — FDA listed —
Total Solutions Hand Sanitizing Wipes 70 g/100g 62819-0448-00 Athea 70 applicators — — FDA listed —
Soft Care Hand Sanitizing Wipes 70 g/100g 64536-1726-06 Diversey, 895 g — — FDA listed —
Instant Hand Sanitizer Wipes 70 mL/100mL 64709-0185-10 Diamond 1 ml — — FDA listed —
Zep Hand Sanitizer Wipes 70 mL 66949-0405-01 Zep 2 swabs — — FDA listed —
Express Wipes Hand Sanitizer 7 g/10g 67858-0645-02 QuestSpecialty 6 canisters — — FDA listed —
Alcohol Disinfecting Wipe 70 mL 68599-5803-04 McKesson 100 packets — — FDA listed —
Hand Sanitizer 70 mL/100mL 70000-0579-01 Cardinal 135 ml — — FDA listed —
Sani Luxe .7 mL/mL 71489-0009-01 Celeste 1.75 ml — — FDA listed —
Signature Care Instant Hand Sanitizizer Wipes 70 g/100g 74149-0112-01 Yiwu 80 pouches — — FDA listed —
Signature Care Instant Hand Sanitizer Wipes 70 g/100g 74149-0113-01 Yiwu 24 pouches — — FDA listed —
Hand Sanitizer Wipes 70 mL/100mL 75214-0501-20 HANUL 134 ml — — FDA listed —
Instant Hand Sanitizizer Wipes 70 g/100g 75262-0201-01 ZheJiang 80 pouches — — Discontinued —
Tazza 70 mL/100mL 76370-0004-00 Tazza 40 applicators — — FDA listed —
Tazza-X Hand Sanitizing Wipes 70 mL/100mL 76370-0008-00 Tazza 180 applicators — — Discontinued —
Tazza-X Extreme Hand Sanitizing Wipes 70 mL/100mL 76370-0010-00 Tazza 50 pouches — — Discontinued —
Singular Wipes 70 mL/100mL 81428-0070-04 SINGULAR 4 ml — — FDA listed —
Singular Wipes lavender fragrance 70 mL/100mL 81428-0072-01 SINGULAR 30 pouches — — FDA listed —
Travel Wipes Moisturizer and fragrance 70 mL/100mL 81428-0074-01 SINGULAR 15 pouches — — FDA listed —
alcohol pad 01 .7 mL 82953-0012-01 Cosmuses 1 cloth — — FDA listed —
Alcohol Cleansing Wipe .7 mL/mL 83165-0001-00 Hubei 1 patch — — FDA listed —
Hand Sanitizing Wipes 70 mL/100mL 83986-0028-64 UpLift 20 packets — — 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

🏛️
2016
On the market since
Apr 2016
📍
2026
Currently FDA-listed
10 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.

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.

Manufacturer & labeler

LabelerProfessional Disposables International Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code10819
First marketedApr 2016
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Professional Disposables International Inc labeler code 10819

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 17 words ▾

Uses Antiseptic. For handwashing to decrease bacteria on the skin. Recommended for repeated use. Dries in seconds.

⏱️ Dosage and Administration 60 words ▾

Directions Peel back label slowly. Pull out wipe and reseal label. Unfold and use. Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry. If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe. Sanitize with a second wipe. Discard after single use.

⚠️ Warnings 38 words ▾

Warnings Flammable, keep away from fire or flame. For external use only. Do not use in or contact the eyes. Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

🧪 Active Ingredient 6 words ▾

Active ingredient Alcohol 70% by volume

🧪 Inactive Ingredients 12 words ▾

inactive ingredients Water, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf juice, Tocopheryl Acetate

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Keep Out of Reach of Children 23 words ▾

Keep this out of reach of children unless under adult supervision. if swallowed, get medical help or contact a Poison Control Center immediately

📄 Package Label / Principal Display Panel 7 words ▾

Principal Display panel Web: Reseal: web reseal

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) — 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 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 Professional Disposables International Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Professional Disposables International 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.
← 10819-3917-01 · Professional 10819-4076-03 · Professional →
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.