MY MEDIC SUPER SANITIZER ETHYL ALCOHOL 75 mL/100mL Gel, 9 mL
by Nantong Health & Beyond Hygienic Products Inc. · .9 mL in 1 PACKET (43473-041-01)
NDC 43473-0041-01
🏷️ FDA NDC (as labeled)
43473-041-01
billing pads the product 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 →
⚠️
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
FDA NDC (as labeled)
43473-041-01
Product NDC
43473-041
11-digit billing NDC
43473004101
RxCUI
1305100
UNII
3K9958V90M
Application #
M005
SPL Set ID
cd8f4ccd-b75e-4de0-87c0-150dfb6e0bf3
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2024-07-02
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 43473-041-01 — 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 → 43473-0041-01. 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.
🏭 Manufacturer & labeler
LabelerNantong Health & Beyond Hygienic Products Inc.
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code43473
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio66 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?
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.
💬 Questions about ETHYL ALCOHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 A7E6112E4N
A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
-
UNII 8Z5ZAL5H3V
A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
-
UNII 09TD8L5SQV
A plant extract from the aloe arborescens species. It functions as a skin-soothing and hydrating ingredient in topical formulations, helping maintain moisture and improve texture.
-
UNII LU49E6626Q
A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
-
UNII 4YK5Z54AT2
Denatonium benzoate is a bitter-tasting chemical compound added to medicines to discourage accidental ingestion, especially by children. It serves as a bittering agent with no therapeutic effect on the body.
-
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 7CVR7L4A2D
A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
-
UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII 4NM5039Y5X
Triclosan is an antimicrobial agent added to medicines to prevent bacterial and fungal growth, helping preserve the product's shelf life and maintain sterility during storage and use.
-
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.
10 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive ingredients Acrylates/C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Fragrance(Parfum), Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Water(Aqua).
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.
💲 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 g | 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Gold Bond Hydrating Hand Sanitizer 75 mL/100mL 41167-0751-02 | Chattem, | 147 ml | — | — | FDA listed | — |
| EVERLIT CARE Hand Sanitizer 75 mL/100mL 43473-0011-01 | Nantong | 9 ml | — | — | FDA listed | — |
| My Medic Super Sanitizer 75 mL/100mLthis 43473-0041-01 | Nantong | 9 ml | — | — | FDA listed | — |
| Unishield Hand Sanitizer 75 mL/100mL 49314-0004-01 | Unishield | 25 packets | — | — | FDA listed | — |
| MedPride Instant Sanitizer 75 mL/100mL 52410-4088-02 | SHIELD | 53 ml | — | — | FDA listed | — |
| Dr. Talbots 75 mL/100mL 70797-0160-01 | Talbots | 50 ml | — | — | FDA listed | — |
| ER Hand Sanitizer Packets 75 mL/100mL 72976-0016-01 | EVER | 114 packets | — | — | FDA listed | — |
| Locke Teddy 75 mL/100mL 73928-0001-01 | KINGKEY | 30 ml | — | — | FDA listed | — |
| Pure care hand sanitizer 75 mL/100mL 73928-0004-01 | KINGKEY | 59 ml | — | — | FDA listed | — |
| livWell 75 mL/100mL 73928-0005-01 | KINGKEY | 30 ml | — | — | FDA listed | — |
| Orbit Innovations Hand Sanitizer 75 mL/100mL 73928-0040-01 | Kingkey | 30 ml | — | — | FDA listed | — |
| Hand Sanitizer .75 mL/mL 74640-0010-30 | Gordon | 30 ml | — | — | FDA listed | — |
| Platinum Hand Sanitizer with Aloe Vera 75 mL/100mL 75262-0002-01 | ZheJiang | 200 ml | — | — | Discontinued | — |
| Hand Sanitiser 75 mL/100mL 75742-0001-01 | Zhejiang | 500 ml | — | — | FDA listed | — |
| Shaboink 75 mL/100mL 75742-0004-01 | Zhejiang | 237 ml | — | — | FDA listed | — |
| H2One 75 mL/100mL 75742-0006-01 | Zhejiang | 237 ml | — | — | FDA listed | — |
| Healing Solutions 75 mL/100mL 75742-0007-01 | Zhejiang | 237 ml | — | — | FDA listed | — |
| Hand Sanitizer Alcohol Hand .75 mL/mL 76892-0001-01 | Design | 1000 ml | — | — | FDA listed | — |
| Instant Free Hand Sanitizer .75 mL/mL 77129-0000-50 | Travel | 50 ml | — | — | FDA listed | — |
| Hand Sanitizer .75 mL/mL 77129-0001-50 | Travel | 50 ml | — | — | FDA listed | — |
| Parasol Scent-Free Hand Sanitizer .75 mL/mL 77446-0001-00 | We've | 500 ml | — | — | FDA listed | — |
| Anti Bacterial Hand Sanitizer .75 mL/mL 78713-0000-02 | MiWorld | 60 ml | — | — | FDA listed | — |
| Hand Sanitizer .75 mL/mL 79401-0001-01 | ORR | 60 ml | — | — | FDA listed | — |
| Instant HAND SANITIZER .75 mL/mL 79524-0000-02 | Xact | 60 ml | — | — | FDA listed | — |
| Hand Sanitizer .75 mL/mL 79631-0000-00 | Andaz | 35 ml | — | — | FDA listed | — |
| hand sanitizer .75 mL/mL 80689-0000-00 | Hygieia | 30 ml | — | — | FDA listed | — |
| EVERLIT CARE Hand Sanitizer 75 mL/100mL 83807-0001-01 | EVERLIT | 9 ml | — | — | FDA listed | — |
| Hand Sanitizer 75 g/100mL 87111-0001-01 | Zhejiang | 30 ml | — | — | FDA listed | — |
| Green Island 75 mL/100mL 75742-0002-01 | Zhejiang | 30 ml | — | — | FDA listed | — |
| MyMedic Super Sanitizer 75 mL/100mL 43473-0307-01 | Nantong | 1.01 ml | — | — | 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.
🔬 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 ETHYL ALCOHOL — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 54%
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 43473-0041-01 You're viewing this | .9 mL in 1 PACKET (43473-041-01) | 2024-07-02 | 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 | ✓ 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 FDA registers it as 43473-041-01, 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: 43473-0041-01, written without dashes as 43473004101. 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 43473-0041-01, the first segment (43473) is the labeler code FDA assigned to Nantong Health & Beyond Hygienic Products Inc.; the middle segment (0041) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 Nantong Health & Beyond Hygienic Products Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Nantong Health & Beyond Hygienic Products 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.
📄 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
🎯 Indications and Usage ▾
Uses to decrease bacteria on the skin thatcould cause disease single use
⏱️ Dosage and Administration ▾
Directions Wet hands thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision. Not recommended for infants
⚠️ Warnings ▾
Warnings For external use only. Flammable, keep away from fire or flame
📦 Storage and Handling ▾
Other information Store at room temperature Do not store above 110F May discolor some fabrics Harmful towood finishes and plastics
🧪 Active Ingredient ▾
Active ingredient Ethyl Alcohol, 75% v/v
🧪 Inactive Ingredients ▾
Inactive ingredients Acrylates/C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Fragrance(Parfum), Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Water(Aqua).
🎯 Purpose ▾
Purpose Antiseptic
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 ↗
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.