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Medline ethyl alcohol 62 mL/100mL Swab — NDC 53329-0121-09 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Medline ethyl alcohol 62 mL/100mL Swab — NDC 53329-121-09 (Billing 53329-0121-09)

by Medline Industries, LP · 1 APPLICATOR in 1 POUCH / 6 mL in 1 APPLICATOR

This is a package of Medline ethyl alcohol 62 mL/100mL Swab from Medline Industries, LP, marketed since Jul 2024 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 53329-0121-09
🏷️ FDA NDC (as labeled) 53329-121-09 billing pads the product segment with a zero
This package
Contains6 mL in 1 applicator Pack sizes2 compare ↓
Main listing for product 53329-121 · Also comes in: 50 pouches 53329-121-29
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

⚠️
Other active recalls for Ethyl Alcohol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 23, 2025 — Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol (Consumer Product Partners, LLC) · FDA recall D-0458-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 53329-121-09
Product NDC 53329-121
11-digit billing NDC 53329012109
RxCUI 1041780
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 11fcc7e7-dfae-ee7d-e063-6294a90a3b31
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-01
Route TOPICAL
Dosage form SWAB
Substance ALCOHOL

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 081343
GCN 48425
HICL code 001681
Ingredient (HICL) Ethyl Alcohol
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5B
Therapeutic class — specific (HIC3) Topical Preparations,Antibacterials
AHFS code 84:04.92.00
AHFS class Local Anti-Infectives, Miscellaneous
FDB label name ETHYL ALCOHOL 62% TOPICAL SWAB
FDB brand name Ethyl Alcohol
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 081343
  • GCN: 48425
  • HICL (First Databank): 001681
  • AHFS class code: 84:04.92.00
  • RxCUI (RxNorm): 1041780
Why two NDCs? The FDA registers this code as 53329-121-09 — 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 → 53329-0121-09. 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

Label name ETHYL ALCOHOL 62% TOPICAL SWAB Ingredient Ethyl Alcohol
📗 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: 50 pouches
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
53329-0121-09 You're viewing this Main listing 1 APPLICATOR in 1 POUCH / 6 mL in 1 APPLICATOR 2024-07-01 — Active
53329-0121-29 53329-121-29 50 POUCH in 1 BOX / 1 APPLICATOR in 1 POUCH / 6 mL in 1 APPLICATOR 2024-07-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 applicator in 1 pouch / 6 ml in 1 applicator.
What NDC number is used to bill for this package of Medline ethyl alcohol 62 mL/100mL Swab?
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
PURELL Hand Sanitizing Wipe 62 mL/100mL 21749-0363-76 GOJO 1 pouch — — FDA listed —
PURELL Cottony Soft Hand Sanitizing Wipe 62 mL/100mL 21749-0364-76 GOJO 1 pouch — — FDA listed —
PURELL Hand Sanitizing Wipes Alcohol Formula 62 mL/100mL 21749-0367-36 GOJO 101 ml — — FDA listed —
Medline 62 mL/100mLthis 53329-0121-09 Medline 1 applicator — — FDA listed —
EO Hand Sanitizer Wipes Lavender 62 mL/100mL 54748-0502-01 EO 3 ml — — FDA listed —
everyone hand sanitizer wipes coconut lemon 62 mL/100mL 54748-0701-15 EO 6 packets — — FDA listed —
everyone hand sanitizer wipes lavender aloe 62 mL/100mL 54748-0702-15 EO 6 packets — — FDA listed —
everyone hand sanitizer wipes ruby grapefruit 62 mL/100mL 54748-0703-15 EO 6 packets — — FDA listed —
CareTouch .62 mL/mL 60913-0026-11 Phoenix 110 packets — — FDA listed —
Hand Sanitizing Wipes .62 mL/mL 60913-0415-11 PHOENIX 110 packets — — FDA listed —
Hand Sanitizing Wipes .62 mL/mL 60913-0416-11 Phoenix 100 packets — — FDA listed —
CareTouch .62 mL/mL 70393-0415-11 Future 110 packets — — FDA listed —
Nozin Nasal Sanitizer (Antiseptic) 62 mL/100mL 82539-0211-02 Global 250 ampules — — FDA listed —
SaniiSwab .62 g/g 84456-0746-02 POLLEY 100 packets — — FDA listed —
SaniiSwab .62 g/g 87051-0001-50 PolleyMed 50 packets — — FDA listed —
SaniiSwab .62 g/g 87051-0002-10 PolleyMed 10 packets — — FDA listed —
GENUINE FIRST AID Antiseptic Hand Sanitizer 62 mL/100mL 43473-0013-01 Nantong 1.03 ml — — FDA listed —
Antiseptic Hand Sanitizer 62 mL/100mL 76138-0113-16 Innovation 1 bottle — — FDA listed —
Hand Sanitizer 62 mL/100mL 83986-0815-16 UpLift 59 ml — — FDA listed —
5253 hand sanitizer 62 mL/100mL 76138-0117-02 Innovation 15 ml — — FDA listed —
Hand Sanitizer Lavender 62 mL/100mL 42681-0010-02 Whole 9 ml — — Discontinued —
Instant Hand Sanitizer 62 mL/100mL 57337-0082-01 Rejoice 53 ml — — FDA listed —
Hillyard Instant Hand Sanitizer 62 mL/100mL 76402-0402-02 Hillyard 1000 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 62 mL/100mL 43473-0089-01 Nantong 9 ml — — FDA listed —
Antibacterial Hand Sanitizer 62 mL/100mL 71513-0105-01 Broder 29.57 ml — — FDA listed —
Thompson Hand Sanitizer 62 mL/100mL 73408-0512-73 Thompson 25 packets — — FDA listed —
Ethyl Alcohol 62 mL/100mL 83986-0969-34 UpLift 236 ml — — FDA listed —
Hand Sanitizer Lavender 62 mL/100mL 42681-7162-02 Whole 946 ml — — FDA listed —
Ethyl alcohol 62 mL/100mL 49035-0418-10 Walmart 29.5 ml — — FDA listed —
Ben E.Keith Hand Cleaner 62 mL/100mL 50980-0056-19 Ben 237 ml — — Discontinued —
Hand Sanitizer 62 mL/100mL 71927-0005-01 Orazen 44 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 71927-0008-01 Orazen 30 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 76138-0114-13 Innovation 30 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 65692-1003-01 Raining 17 ml — — FDA listed —
5259 Hand Sanitizer 62 mL/100mL 76138-0120-04 Innovation 40 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 62 mL/100mL 83807-0003-01 EVERLIT 9 ml — — FDA listed —
Moisturizing Hand Sanitizer 62 mL/100mL 83986-0447-45 UpLift 1150 ml — — FDA listed —
Instant Hand Sanitizer 62 mL/100mL 57337-0084-01 Rejoice 53 ml — — FDA listed —
Lightning X Hand Cleanser 62 mL/100mL 43473-0122-01 Nantong 9 ml — — FDA listed —
5406 hand sanitizer 62 mL/100mL 76138-0116-03 Innovation 30 ml — — FDA listed —
Moisturizing Hand Sanitizer 62 mL/100mL 83986-0849-16 UpLift 59 ml — — FDA listed —
Spectrum 62% Hand Sanitizer 62 mL/100mL 53329-0214-13 Medline 59.147 ml — — Discontinued —
Instant Hand Sanitizer 62 mL/100mL 57337-0083-01 Rejoice 53 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 71927-0001-01 Orazen 30 ml — — Discontinued —
Frosted Cherry Scented Hand Sanitizer 62 mL/100mL 60193-0001-00 Pacific 1 bottle — — FDA listed —
Gingerbread Scented Hand Sanitizer 62 mL/100mL 60193-0002-00 Pacific 1 bottle — — 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

🏛️
2024
On the market since
Jul 2024
📍
2026
Currently FDA-listed
2 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 QN83US2B0N
    Ascorbyl palmitate is a fat-soluble form of vitamin C used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down and becoming less stable over time.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII D5340Y2I9G
    Castor oil is a natural plant-based oil used in medicines as a lubricant, laxative agent, and solvent. It helps medicine ingredients dissolve or flow smoothly and can aid bowel movement in formulations designed for that purpose.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII DT9D8Z79ET
    Polyaminopropyl biguanide is a synthetic antimicrobial agent used as a preservative in liquid medicines and topical products. It helps prevent bacterial and fungal growth during storage.
  • 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.

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

The official label also statesascorbyl palmitate, benzyl alcohol, BHT, castor (ricinus communis) oil, fragrance, isopropyl alcohol, menthol, polyaminopropyl biguanide, purified 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

LabelerMedline Industries, LP
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code53329
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio120 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
🎯 Indications and Usage 10 words ▾

Uses helps reduce bacteria that potentially can cause skin infections

⏱️ Dosage and Administration 5 words ▾

Directions Swab locally as needed.

⚠️ Warnings 81 words ▾

Warnings For external use only. Flammable. Keep away from heat or flame.

Do not use in the eyes on children under 2 years of age unless directed by a doctor Ask a doctor before use if injuries are deep or puncture wounds serious burns Stop and ask a doctor if redness, irritation, swelling or pain persists or increases infection occurs Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

🧪 Active Ingredient 6 words ▾

Active ingredient Ethyl Alcohol 62% v/v

🧪 Inactive Ingredients 19 words ▾

Inactive ingredients ascorbyl palmitate, benzyl alcohol, BHT, castor (ricinus communis) oil, fragrance, isopropyl alcohol, menthol, polyaminopropyl biguanide, purified water

🎯 Purpose 2 words ▾

Purpose Antiseptic

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 Medline Industries, LP. 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 50 pouches (53329-0121-29). 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?
Medline Industries, LP 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.
← 53329-0120-05 · Medline 53329-0125-09 · Medline →
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.