Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Instant Hand Sanitizeing Wipe Isopropanol and Compound double-stranded quaternary ammonium salts 1.2 g Cloth, 50-count — NDC 79539-002-05 (Billing 79539-0002-05)
by Shandong Yayun Sanitary Products Co., Ltd. · 50 CLOTH in 1 BAG
This is a package of 50 cloths of Instant Hand Sanitizeing Wipe Isopropanol and Compound double-stranded quaternary ammonium salts 1.2 g Cloth from Shandong Yayun Sanitary Products Co., Ltd., marketed since Mar 2020 and currently FDA-listed.
NDC 79539-0002-05
🏷️ FDA NDC (as labeled)
79539-002-05
billing pads the product segment with a zero
This package
Contains50-count
Pack sizes24 compare ↓
Product page 79539-0002-01
Also comes in:
10 cloths 79539-002-01
20 cloths 79539-002-02
30 cloths 79539-002-03
40 cloths 79539-002-04
60 cloths 79539-002-06
70 cloths 79539-002-07
80 cloths 79539-002-08
100 cloths 79539-002-09
120 cloths 79539-002-10
150 cloths 79539-002-11
160 cloths 79539-002-12
180 cloths 79539-002-13
200 cloths 79539-002-14
300 cloths 79539-002-15
400 cloths 79539-002-16
500 cloths 79539-002-17
600 cloths 79539-002-18
700 cloths 79539-002-19
800 cloths 79539-002-20
1000 cloths 79539-002-21
1200 cloths 79539-002-22
1600 cloths 79539-002-23
2000 cloths 79539-002-24
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
79539-002-05
Product NDC
79539-002
11-digit billing NDC
79539000205
UNII
6DC9Q167V3
Application #
M003
SPL Set ID
aa0dc01a-2c6b-7402-e053-2a95a90af6a2
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-03-30
Route
TOPICAL
Dosage form
CLOTH
Substance
PROPYLENE GLYCOL
Why two NDCs?
The FDA registers this code as 79539-002-05 — 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 → 79539-0002-05. 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
🧪 What is this product?
This is a topical hand sanitizing wipe marketed as an over-the-counter monograph product. The cloth is moistened with propylene glycol, which is commonly used in sanitizing products as a humectant and antimicrobial agent. The wipe is intended for topical application to the skin as a convenient way to clean and sanitize hands, particularly in settings where soap and water are not readily available.
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.
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
💬 Questions about Isopropanol and Compound double-stranded quaternary ammonium salts?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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.
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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 79539-0002-01 79539-002-01 Main listing | 10 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-02 79539-002-02 | 20 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-03 79539-002-03 | 30 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-04 79539-002-04 | 40 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-05 You're viewing this | 50 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-06 79539-002-06 | 60 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-07 79539-002-07 | 70 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-08 79539-002-08 | 80 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-09 79539-002-09 | 100 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-10 79539-002-10 | 120 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-11 79539-002-11 | 150 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-12 79539-002-12 | 160 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-13 79539-002-13 | 180 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-14 79539-002-14 | 200 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-15 79539-002-15 | 300 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-16 79539-002-16 | 400 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-17 79539-002-17 | 500 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-18 79539-002-18 | 600 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-19 79539-002-19 | 700 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-20 79539-002-20 | 800 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-21 79539-002-21 | 1000 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-22 79539-002-22 | 1200 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-23 79539-002-23 | 1600 CLOTH in 1 BAG | 2020-03-30 | — | Active |
| 79539-0002-24 79539-002-24 | 2000 CLOTH in 1 BAG | 2020-03-30 | — | Active |
You're viewing one of 24 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This is a 50-count package — 50 cloth in 1 bag.
How does this package differ from NDC 79539-0002-01?
Both are Instant Hand Sanitizeing Wipe Isopropanol and Compound double-stranded quaternary ammonium salts 1.2 g Cloth — the drug itself is identical. This page's package is the 50-count one, while NDC 79539-0002-01 is the 10 cloths package.
What NDC number is used to bill for this package of Instant Hand Sanitizeing Wipe Isopropanol and Compound double-stranded quaternary ammonium salts 1.2 g 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Instant Hand Sanitizeing Wipe 1.2 gthis 79539-0002-05 | Shandong | 50 cloths | — | — | 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2020
On the market since
Mar 2020
📍
2026
Currently FDA-listed
6 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.
- FDA Orange Book · refreshed Sep 3, 2026
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 9E8X80D2L0
A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
-
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 F5UM2KM3W7
Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
-
UNII D9OM4SK49P
Cetylpyridinium chloride is a chemical compound that acts as a preservative and antimicrobial agent in medicines. It helps prevent bacterial growth and extends the shelf life of liquid formulations.
-
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 7FLD91C86K
Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
-
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 HIE492ZZ3T
Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
-
UNII 1Q73Q2JULR
Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
-
UNII 64B59K7U6Q
A reactive chemical compound used as a fumigant and sterilizing agent. In medicines, it may serve to sterilize equipment, containers, or manufacturing environments rather than as a direct ingredient in the final product.
-
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.
11 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWATER SODIUM CITRATE Compound double-stranded quaternary ammonium salt
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
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
LabelerShandong Yayun Sanitary Products Co., Ltd.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code79539
First marketedMar 2020
Product typeHuman Otc Drug
Portfolio3 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
📄 Do Not Use
📄 When Using This Product
📄 Stop Use and Ask a Doctor If
📄 Keep Out of Reach of Children
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Use Instant Hand Sanitizeing Wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
⏱️ Dosage and Administration ▾
Directions Wipe the surface of the skin and let it dry naturally. Supervise children under 6 years of age when using this product to avoid swallowing.
⚠️ Warnings ▾
Warnings For external use only. Flammable. Keep away from heat or flame
📦 Storage and Handling ▾
Other information Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
🧪 Active Ingredient ▾
Active Ingredient(s) BENZALKONIUM CHLORIDE 1.2g/pcs. Purpose: Antiseptic
🧪 Inactive Ingredients ▾
Inactive ingredients WATER SODIUM CITRATE Compound double-stranded quaternary ammonium salt
🎯 Purpose ▾
Purpose Antiseptic, Instant Hand Sanitizeing Wipe
📄 Do Not Use ▾
Do not use in children less than 2 months of age on open skin wounds
📄 When Using This Product ▾
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
Package Label - Principal Display Panel 2
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 ↗
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 Instant Hand Sanitizeing Wipe (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 55%
Female · 45%
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.
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 Shandong Yayun Sanitary Products Co., Ltd.. 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 23 other package presentations of this same product, including 10 cloths (79539-0002-01), 20 cloths (79539-0002-02), 30 cloths (79539-0002-03). 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?
Shandong Yayun Sanitary Products Co., Ltd. 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.
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.