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Germ-Away Anti-microbial 1 mg/g Cloth, 80 g — NDC 74680-0107-46 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Germ-Away Anti-microbial 1 mg/g Cloth, 80 g — NDC 74680-107-46 (Billing 74680-0107-46)

by Unico International Trading Corp · 80 g in 1 CANISTER

This is a package of 80 g of Germ-Away Anti-microbial 1 mg/g Cloth from Unico International Trading Corp, marketed since Jun 2020 and currently FDA-listed. It is this product's only package size.

NDC 74680-0107-46
🏷️ FDA NDC (as labeled) 74680-107-46 billing pads the product 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 74680-107-46
Product NDC 74680-107
11-digit billing NDC 74680010746
RxCUI 1038856
UNII F5UM2KM3W7
Application # M003
SPL Set ID a7d0ce42-9076-143c-e053-2995a90aeeb6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-11
Route TOPICAL
Dosage form CLOTH
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1038856
Why two NDCs? The FDA registers this code as 74680-107-46 — 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 → 74680-0107-46. 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 Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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

🧪 What is this product?

Germ-Away Anti-microbial is a cloth saturated with benzalkonium chloride, a type of antimicrobial agent applied directly to the skin. This product is marketed as an over-the-counter monograph drug, meaning it is sold under FDA's established rules for this category of antimicrobial cloths rather than through an individual product application. Benzalkonium chloride is typically used in topical products to help reduce bacteria and other microorganisms on the skin surface.

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
74680-0107-46 You're viewing this Main listing 80 g in 1 CANISTER 2020-06-11 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
5EWA5 Antibacterial Hand Sanitizer Wipes .1 g/100g 40096-1909-01 W.W. 6 canisters — — Discontinued —
SCRUBS Hand Sanitizer Wipes .1 g/100g 51239-2909-01 ITW 400 g — — FDA listed —
Aerowipe .1 g/100g 55305-0118-10 Aero 1.5 g — — FDA listed —
Hand Sanitizing Wipes 1 mg/g 69446-0220-00 Ez 1500 patches — — FDA listed —
GERMisept Antibacterial Hand Sanitizing Wipes 1 mg/mL 70335-0012-01 Innovent 200 patches — — FDA listed —
Redicare Antiseptic Towelettes 1 mg/1000mg 71105-0800-02 Redicare 50 packets — — FDA listed —
Klean-Them Hand Sanitizing Towels .1 g/100g 73943-0953-01 Rite-Kem, 400 g — — FDA listed —
Nuvik Large Roll in Bucket Antibacterial Hand Wipes .1 g/100mL 74602-0900-80 Nuvik 1 pail — — FDA listed —
Germ-Away 1 mg/gthis 74680-0107-46 Unico 80 g — — FDA listed —
Germ-Away 1 mg/g 74680-0110-23 Unico 72 g — — FDA listed —
Germ-Away 1 mg/g 74680-0111-45 Unico 80 g — — FDA listed —
Germ-Away 1 mg/g 74680-0112-88 Unico 1200 g — — FDA listed —
Pet wipes 1 g 79539-0801-01 Shandong 1 cloth — — FDA listed —
CleanCom .01 mg 80436-0005-01 RMT 200 cloths — — Discontinued —
Theraplus Antibacterial Wipes Fresh Scent with Aloe and Vitamin E 1 mg/mL 80684-0007-20 Fourstar 20 patches — — Discontinued —
wet wipes 01 .1 g/1001 82953-0048-01 Cosmuses 10 cloths — — FDA listed —
fomin mini Hand Sanitizer Wipes COCO-NILLA BLISS .1 g/100mL 85755-0001-08 Fomin 6 packets — — FDA listed —
fomin mini Hand Sanitizer Wipes MELON POP .1 g/100mL 85755-0002-08 Fomin 6 packets — — FDA listed —
fomin mini Hand Sanitizer Wipes FRAGRANCE FREE .1 g/100mL 85755-0003-08 Fomin 6 packets — — FDA listed —
fomin mini Hand Sanitizer Wipes - 6 - VARIETY PACK 85755-0004-06 Fomin 1 kit — — 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

🏛️
2020
On the market since
Jun 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.

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 7KOI7K0DHI
    A synthetic liquid alcohol used as a solvent and humectant in medicines. It helps dissolve active ingredients and maintain moisture in liquid formulations.
  • UNII DPY9K1927C
    3,7-Dimethyl-1-octanol is a fatty alcohol derived from natural sources or synthesized chemically. It acts as an emollient and solvent in medications, helping to dissolve or suspend active ingredients and improve how the product feels on skin or mucous membranes.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • 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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • 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 A4VZ22K1WT
    Coumarin is a fragrant organic compound derived from plants or made synthetically. It adds pleasant flavor and aroma to medicines and is used as a flavoring agent in some formulations.
  • UNII CEB8Q6WHK2
    A salt derived from formic acid, used in pharmaceutical formulations as a buffer or pH adjuster to maintain the proper acidity level of the medicine.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII 3O695R5M1U
    Diphenyl ether is an organic compound used as a solvent and preservative in medicines. It helps dissolve active ingredients and protect the product from spoiling during storage.
  • UNII MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • UNII RV6J6604TK
    Eucalyptol is a natural oil compound extracted from eucalyptus plants. In medicines, it serves as a flavoring agent and aromatic component to improve taste and smell.
  • 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII ZEL54N6W95
    A silicone-based compound that helps oils and water mix together. Used in medicines as an emulsifier and anti-foaming agent to improve texture and prevent bubbles in liquids and creams.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII DIG6BWZ9XT
    Sodium hydroxymethylglycinate is a preservative that prevents bacterial and fungal growth in liquid medicines and personal care products. It works by releasing formaldehyde in small amounts to keep the product stable and safe during storage.
  • UNII UM4XS5M134
    A synthetic fragrance ingredient derived from linalool, a naturally occurring compound found in plants. It functions as a fragrance component and masking agent to improve the smell and taste appeal of the medicine.
  • 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.

21 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate, fragrance

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

LabelerUnico International Trading Corp
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code74680
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio9 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 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 31 words ▾

Directions Pull one sheet from canister at an angle. Sanitize hands or other affected area. Discard in trash after use. Do not flush. Close lid flap after use to retain moisture.

⏱️ Dosage and Administration 61 words ▾

To dispense Pop off canister lid. Remove seal. Pull up corner of center sheet and thread wipe through lid opening. Snap lid back onto the canister. To Use: Pull one sheet from canister at an angle and snap off. Clean hands or affected area and discard in trash after use. Do not flush. Close lid flap after use to retain moisture.

⚠️ Warnings 49 words ▾

Warnings For external use only. Do not use in the eyes. Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult doctor if irritation persists for more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.1%

🧪 Inactive Ingredients 33 words ▾

Inactive Ingredients Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate, fragrance

🎯 Purpose 2 words ▾

Purpose Anti-bacterial

📄 Keep Out of Reach of Children 17 words ▾

Keep out of the reach of children. Keep out of reach of children, except with adult supervision.

📄 Package Label / Principal Display Panel 4 words ▾

Package Label Germ-Away 80

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 Unico International Trading Corp. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Unico International Trading Corp 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.
← 74680-0104-15 · Unico 74680-0108-11 · Unico →
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.