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Deconimo HAND SANITIZING WIPES 75 mL/100mL Cloth

by IMAGINE AMAZON LLC · 50 PACKET in 1 PACKET (85380-0002-2) / 100 mL in 1 PACKET (85380-0002-1)
NDC 85380-0002-02
🏷️ FDA NDC (as labeled) 85380-0002-2 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 85380-0002-2
Product NDC 85380-0002
11-digit billing NDC 85380000202
RxCUI 1307051
UNII 3K9958V90M
UPC 0198168926529
Application # M003
SPL Set ID 311c670d-8f87-b746-e063-6294a90afd5e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-03-01
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 85380-0002-2 — 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 → 85380-0002-02. 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

LabelerIMAGINE AMAZON LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code85380
First marketedMar 2025
Product typeHuman Otc Drug
Portfolio2 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?
📖 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.

🧪 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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Jianerkang Wipes .75 mL/mL 34645-0004-01 Jianerkang 50 pouches — — FDA listed —
BBlove ALCOHOL WIPES 75 g/1001 43116-0035-01 Shenzhen 50 cloths — — FDA listed —
BBlove ALCOHOL WIPES 75 U/100U 43116-0038-01 Shenzhen 1 u — — FDA listed —
Beautifier Life ALCOHOL WIPES 75 U/100U 43116-0039-01 Shenzhen 1 u — — FDA listed —
Alcohol Wipes 75 U/100U 43116-0050-01 Shenzhen 50 us — — FDA listed —
MedPride Alcohol Wipes .75 g 52410-4105-05 Shield 100 cloths — — FDA listed —
Good to Go Alcohol Wipes 75 g/100g 67751-0200-01 Navajo 15 pouches — — Discontinued —
Good to Go Alcohol Wipes 15ct 75 g/100g 67751-0238-15 Navajo 15 pouches — — FDA listed —
Germisept Antibacterial Hand Sanitizing Alcohol Wipes .75 mL/mL 70335-0010-01 Innovent, 150 patches — — FDA listed —
GERMisept Antibacterial Hand Sanitizing Alcohol Wipes 75 mL/100mL 70335-0011-01 Innovent 200 patches — — FDA listed —
ONID Wipe 75 mL/100mL 71441-0180-10 ONID 82 ml — — FDA listed —
Novo wipe 75 g/100g 71734-0262-01 JIANGMEN 3.7 g — — FDA listed —
Locke Teddy 75 mL/100mL 73928-0006-01 KINGKEY 1 pouch — — FDA listed —
Hand Sanitizer Wipes 75 mL/100mL 75214-0503-10 HANUL 134 ml — — FDA listed —
Hand Sanitizer Wipes 75 g/1001 75428-0035-01 Shandong 80 cloths — — FDA listed —
Deyo .75 mL 75622-0633-10 Henan 10 cloths — — FDA listed —
Deeyeo .75 mL 75622-0677-80 Henan 80 cloths — — FDA listed —
SnugZ Hand Sanitizing Wipes 75 mL/100mL 76309-0700-85 SnugZ/USA, 38.75 ml — — FDA listed —
Fight wipes .75 mL/mL 77133-0001-01 ALCOVE 20 patches — — Discontinued —
O Well sanitizing hand wipes .75 mL/mL 77133-0002-01 ALCOVE 20 patches — — Discontinued —
Alcohol Wipes 75 mL/100mL 77412-0199-01 Shandong 50 patches — — Discontinued —
Hygienic Instant Hand Sanitizing Wipes .75 mL/mL 77462-0010-01 SORA 80 patches — — FDA listed —
Alcohol Wipes 75 mL/100mL 77665-0104-01 Guangzhou 80 ml — — FDA listed —
SFT1 Sanitizing Wipes .75 mL/mL 79401-0002-50 ORR 50 patches — — FDA listed —
Alcohol Pad .75 mL/mL 80139-0102-01 Foshan 4 ml — — Discontinued —
Alcohol Wipes .75 mL/mL 81079-0002-01 Shaoxing 38 ml — — FDA listed —
Alcohol Wipes 75 mL/100mL 81079-0003-01 Shaoxing 80 ml — — FDA listed —
Singular Wipes fresh Citrus Scent 75 mL/100mL 81428-0081-01 SINGULAR 30 pouches — — FDA listed —
Travel Wipes Fresh Citrus Scent 75 mL/100mL 81428-0084-01 SINGULAR 30 pouches — — FDA listed —
NSI Sanitizing Wipes 75 mL/g 82716-0000-50 NORTHERN 50 patches — — FDA listed —
PentaCleanse Alcohol Wipes 75 mL/100mL 82901-0002-02 Prestige 60 patches — — FDA listed —
Hua Jing Alcohol Prep Pad .75 mL/mL 83170-0001-02 Hua 100 patches — — FDA listed —
Hua Jing Alcohol Prep Pad (Thick) .75 mL/mL 83170-0002-02 Hua 100 patches — — FDA listed —
Hand Sanitizing Wipes 75 mL/100mL 84973-0075-01 Germs 176 ml — — FDA listed —
MagiCare Premium Hand Sanitizing Wipes 75 mL/100mL 85276-0104-01 MAGICARE 20 patches — — FDA listed —
Hand Sanitizing Wipes 75 mL/100mL 85380-0001-02 IMAGINE 50 packets — — FDA listed —
Deconimo 75 mL/100mLthis 85380-0002-02 IMAGINE 50 packets — — FDA listed —
Refreshify Antiseptic Hand Wipes 87031-0000-00 Emes 80 patches — — FDA listed —
Refreshify Antiseptic Hand Wipes 75 mL/100mL 87031-0003-01 Emes 1 patch — — FDA listed —
WIDESPREAD Hand Sanitizing Wipes 75 mL/100mL 87145-0001-02 HAMAOUI 400 patches — — FDA listed —
Alcohol wipes Hand Sanitizing Wipes .75 mL/mL 87159-0001-80 DGE 80 patches — — 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

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85380-0002-02 You're viewing this 50 PACKET in 1 PACKET (85380-0002-2) / 100 mL in 1 PACKET (85380-0002-1) 2025-03-01 Active

🧭 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 — Not published for this NDC No photo available yet for this listing.
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 FDA registers it as 85380-0002-2, 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: 85380-0002-02, written without dashes as 85380000202. 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 85380-0002-02, the first segment (85380) is the labeler code FDA assigned to IMAGINE AMAZON LLC; the middle segment (0002) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 IMAGINE AMAZON LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
IMAGINE AMAZON LLC 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 43 words ▾

Directions Open lid, gently pull back resealable label, remove and use wipe as required. •Reseal back after use to avoid evaporation of alcohol. Other informations • Store at room temperature 15°C-30°C(59°F-86°F). Lot No. Manufacture date and Expiration date can be found on package.

⏱️ Dosage and Administration 27 words ▾

Uses For hand sanitizing to decrease bacteria on the skin. Purpose .Antiseptic Apply topically to the skin to help prevent cross contamination. Not recommended for repeated use.

⚠️ Warnings 56 words ▾

Warnings • Flammable, keep away from fire or flame. For external use only. • Do not use in contact the eyes. Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases. • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 6 words ▾

Active Ingredient Alcohol 75% by volume

🧪 Inactive Ingredients 1 words ▾

Water

🎯 Purpose 27 words ▾

Uses For hand sanitizing to decrease bacteria on the skin. Purpose .Antiseptic Apply topically to the skin to help prevent cross contamination. Not recommended for repeated use.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85380-0001-02 · IMAGINE 85380-1001-01 · Image →
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.