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All-Health Wound Care Kit ethyl alcohol Kit — NDC 51142-0003-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

All-Health Wound Care Kit ethyl alcohol Kit — NDC 51142-003-01 (Billing 51142-0003-01)

by ASO LLC · 1 KIT in 1 CASE * .0019 L in 1 PACKET

This is a package of All-Health Wound Care Kit ethyl alcohol Kit from ASO LLC, marketed since Aug 2019 and currently FDA-listed. It is this product's only package size.

NDC 51142-0003-01
🏷️ FDA NDC (as labeled) 51142-003-01 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

⚠️
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) 51142-003-01
Product NDC 51142-003
11-digit billing NDC 51142000301
RxCUI 1039699
Application # 505G(a)(3)
SPL Set ID 939ff14f-bdfe-408a-bc4b-71da3bae194d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-08-21
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1039699
Why two NDCs? The FDA registers this code as 51142-003-01 — 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 → 51142-0003-01. 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.

Clinical

🧪 What is this product?

This is an over-the-counter wound care kit that contains ethyl alcohol as its active ingredient. Ethyl alcohol is commonly used in wound care products as an antimicrobial agent to help reduce bacteria on the skin around minor cuts, scrapes, and wounds. The kit format allows consumers to have alcohol and other wound care supplies together for cleaning and preparing skin before minor first aid treatment.

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
51142-0003-01 You're viewing this Main listing 1 KIT in 1 CASE * .0019 L in 1 PACKET 2019-08-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Bcbgeneration 4 Pc Hand Sanitizers - Cherry Blossom, Brown Sugar Vanilla, Velvet Peach And Ocean Breeze Scent 87247-0590-04 Diamond 1 kit — — FDA listed —
All-Health Wound Care Kitthis 51142-0003-01 ASO 1 kit — — FDA listed —
Bcbgeneration Hand Sanitizer Mist Set-Mango, Berry, Strawberry And Vanilla Scent 69933-0301-02 Pearl 1 kit — — FDA listed —
Smart Care 3 HAND SANITIZER 1.35 FL OZ (CHERRY KISS, SPARKLING GUAVA, RASPBERRY SWIRL) 70108-0217-01 Ashtel 1 kit — — FDA listed —
Sour Lemon Hand Sanitizer Trio - Sweet Cherry, Toasted Marshmallow And Sugar Macaron Scent 87247-0014-03 Diamond 1 kit — — FDA listed —
SOUR LEMON 2 PACK Hand Sanitizer - WATERMELON AND SWEET CHERRY SCENT 87247-0935-02 Diamond 1 kit — — FDA listed —
Bcbg Generation Hand Sanitizer Duo - Velvet Peach And Brown Sugar Vanilla Scent 87247-0931-02 Diamond 1 kit — — FDA listed —
Bcbgeneration Hand Sanitizer Mist Set-Mango And Strawberry Scent 69933-0309-02 Pearl 1 kit — — FDA listed —
Sour Lemon 2 Pc Hand Sanitizer With Stickers - Salted Caramel And Souffle Vanilla Scent 87247-0017-02 Diamond 1 kit — — FDA listed —
SOUR LEMON 4 PACK Hand Sanitizer - WATERMELON, VANILLA, SWEET CHERRY AND CUCUMBER MELON SCENT 87247-0589-04 Diamond 1 kit — — FDA listed —
BCBG GENERATION HAND SANITIZER DUO - WILD Cherry AND Mango Cherry SCENT 87247-0933-02 Diamond 1 kit — — FDA listed —
Smart Care WATERMELON HAND SANITIZER AND LIP GLOSS SET 70108-0342-01 Ashtel 1 kit — — FDA listed —
meijer 3 Hand Sanitizers 1 FL OZ (SUGAR COOKIE, PEPPERMINT, GINGERBREAD) 79481-0393-01 Meijer, 1 kit — — FDA listed —
BCBG GENERATION HAND SANITIZER DUO - MALIBU Peach and PINK Guava SCENT 87247-0926-02 Diamond 1 kit — — FDA listed —
Bcbg Generation 2 Pc Hand Sanitizer Mist - Berry And Vanilla Scent 87247-0928-02 Diamond 1 kit — — FDA listed —
Bcbgeneration Hand Sanitizer Trio - Peony Blush, Amber And Lavender, Coconut Water Scent 87247-0956-03 Diamond 1 kit — — FDA listed —
Smart Care 3 HAND SANITIZERS 1.35 FL OZ (OCEAN, CEDAR and CYPRESS, SANDALWOOD) 70108-0266-01 Ashtel 1 kit — — FDA listed —
SMART CARE Polly Pocket HAND SANITIZER AND LIP GLOSS SET 70108-0329-01 Ashtel 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

🏛️
2019
On the market since
Aug 2019
📍
2026
Currently FDA-listed
7 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.

From the label’s inactive-ingredient sectionaloe vera, fragrance, purified water, triethanolamine

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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.

Manufacturer & labeler

LabelerASO LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code51142
First marketedAug 2019
Product typeHuman Otc Drug
Portfolio8 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 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

Uses – Antiseptic Wipes • Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

⏱️ Dosage and Administration 25 words ▾

Directions – Antiseptic Wipes • tear open packet, remove towelette • unfold and use as a washcloth • supervise children under 6 years of age

⚠️ Warnings 74 words ▾

Warnings – Antiseptic Wipes For external use only Flammable: keep away from fire or flame Do not use – Antiseptic Wipes in the eyes. If this happens, rinse thoroughly with water. Stop use and ask a doctor – Antiseptic Wipes if irritation or redness develop and persists for more than 72 hours Keep out of reach of children – Antiseptic Wipes If swallowed get medical help or contact a Poison Control Center right away

🧪 Active Ingredient 8 words ▾

Active ingredients – Antiseptic Wipes Ethyl Alcohol 66.5%

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients – Antiseptic Wipes aloe vera, fragrance, purified water, triethanolamine

🎯 Purpose 5 words ▾

Purpose – Antiseptic Wipes Antiseptic

📄 Do Not Use 16 words ▾

Do not use – Antiseptic Wipes in the eyes. If this happens, rinse thoroughly with water.

📄 Stop Use and Ask a Doctor If 21 words ▾

Stop use and ask a doctor – Antiseptic Wipes if irritation or redness develop and persists for more than 72 hours

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children – Antiseptic Wipes If swallowed get medical help or contact a Poison Control Center right away

📄 Other Information 128 words ▾

Other Safety Information – All-Health Wound Care Kit 3-STEP WOUND CARE KIT FOR SMALL TO MEDIUM SIZED WOUNDS For wound sites ranging in size from 1 INCH - 3 INCH which may include: • Common Wounds • Lacerations • Abrasions • Minor burns Dressings may be cut or folded for specific wound size. Not made with natural rubber latex. Gauze Pads, Non-Stick Pads, Transparent Dressings, and Rolled Gauze are sterile unless individual wrapper has been opened or damaged.

Paper Tape and Antiseptic Wipes are non-sterile. Gauze Pads and Rolled Gauze are Rayon-polyester bend. Consult with your medical professional for specific treatment of wound site and proper dressing change procedures.

WARNING: In case of deep puncture wounds, serious burns, or signs of infection, consult a physician. Single use only.

📄 Package Label / Principal Display Panel 106 words ▾

Principal Display Panel – All-Health Wound Care Kit ALL-HEALTH ® WOUND CARE PRODUCTS 3-STEP WOUND CARE KIT FOR SMALL TO MEDIUM SIZED WOUNDS Essential items to support 3-STEP WOUND CARE: CLEAN COVER SECURE • For 1 IN to 3 IN wound sites • 7 – 10 days of use 40 ITEMS SEE BACK PANEL FOR KIT CONTENTS ALL-HEALTH ® is an ASO brand Distributed by ASO LLC Sarasota, Fl 34240 | www.asocorp.com Label image-01

Principal Display Panel – Antiseptic Wipes Safetec Antiseptic Towelette For Professional and Hospital Use Contents: 1 single-use, premoistened towelette Manufactured by SAFETEC OF AMERICA, Inc. Buffalo, NY 14215 800-456-7077 www.safetec.com Label image-03

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 All-Health Wound Care Kit (this brand).

Top reported reactions

Drug Abuse48
Toxicity To Various Agents31
Overdose27
Intentional Overdose19
Poisoning Deliberate19
Suicide Attempt19
Completed Suicide18

Age at onset

Adolescent2
Adult30
Elderly5

Reporter sex

236 reports
Male · 61%
Female · 39%

Serious outcomes

Hospitalization99
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 23 0
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 Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 ASO LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ASO 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.
← 51141-0701-05 · NeoPharm 51142-0005-01 · ASO →
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.