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Isopro First Aid Isopropyl Alcohol 70 mL/100mL Spray — NDC 59898-0402-15 package photo

Isopro First Aid Isopropyl Alcohol 70 mL/100mL Spray

by Water-Jel Technologies · 24 BOTTLE, SPRAY in 1 CASE (59898-402-15) / 59 mL in 1 BOTTLE, SPRAY (59898-402-10)
NDC 59898-0402-15
🏷️ FDA NDC (as labeled) 59898-402-15 billing pads the product segment with a zero
This package
Contains59 mL in 1 bottle, spray Pack sizes2 compare ↓
Also comes in: 59 ml 59898-0402-10
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

⚠️
Other active recalls for Isopropyl Alcohol (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0373-2026
Class II · Jul 7, 2025 — Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. (MEDLINE INDUSTRIES, LP - Northfield) · FDA recall D-0604-2025
Class II · Jul 7, 2025 — Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. (MEDLINE INDUSTRIES, LP - Northfield) · FDA recall D-0601-2025
Class II · Jul 7, 2025 — Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. (MEDLINE INDUSTRIES, LP - Northfield) · FDA recall D-0602-2025
Class II · Jul 7, 2025 — Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. (MEDLINE INDUSTRIES, LP - Northfield) · FDA recall D-0600-2025
Class II · Jul 7, 2025 — Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. (MEDLINE INDUSTRIES, LP - Northfield) · FDA recall D-0605-2025
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 59898-402-15
Product NDC 59898-402
11-digit billing NDC 59898040215
RxCUI 1014638
UNII ND2M416302
UPC 0743537500031
Application # M003
SPL Set ID f38563f5-ee54-4979-9157-4bf8fd60daab
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-05-23
Route TOPICAL
Dosage form SPRAY
Substance ISOPROPYL ALCOHOL
Why two NDCs? The FDA registers this code as 59898-402-15 — 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 → 59898-0402-15. 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
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

LabelerWater-Jel Technologies
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code59898
First marketedMay 2010
Product typeHuman Otc Drug
Portfolio18 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

🧪 What is this product?

This is a topical spray containing 70% isopropyl alcohol, sold as an over-the-counter antiseptic product under FDA's OTC monograph rules. Isopropyl alcohol is commonly used on skin to help reduce bacteria and germs before minor medical procedures, wound cleaning, or injection sites. The spray form allows for easy application to affected areas. This product is not individually approved by the FDA but is marketed under the established regulatory framework for OTC antiseptic drugs.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also stateswater

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 systemPer mLPer 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: 59 ml
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
Isopropyl Alcohol 70 mL/100mL 35418-0402-10 Zee 59 ml — — FDA listed —
Xpect Isopropyl Alcohol 70 mL/100mL 42961-0201-01 Cintas 59.1 ml — — FDA listed —
Medi-First Isopropyl Alcohol 70 mL/100mL 47682-0262-02 Unifirst 59.1 ml — — FDA listed —
Medi-First Isopropyl Alcohol 70% 70 mL/100mL 47682-0263-02 Unifirst 59.1 ml — — FDA listed —
Medi-First Isopropyl Alcohol 70% 70 mL/100mL 47682-0264-02 Unifirst 59.1 ml — — FDA listed —
Green Guard Isopropyl Alcohol 70% 70 mL/100mL 47682-0315-02 Unifirst 59.1 ml — — FDA listed —
Alcohol 70 mL/100mL 50332-0213-01 NorMed 60 ml — — FDA listed —
Alcohol 70 mL/100mL 50332-0223-01 NorMed 59 ml — — FDA listed —
70% 70 mL/100mL 50804-0810-08 Perrigo 3785 ml — — Discontinued —
CVS Health Isopropyl Rubbing Alcohol 70 mL/100g 51316-0979-00 CVS 85 g — — FDA listed —
American Red Cross 70 Isopropyl Alcohol 70 mL/100g 51628-0030-00 My 70 g — — FDA listed —
American Red Cross 70 Isopropyl Alcohol with Continuous Nitrogen Gas 70 mL/100g 51628-0031-00 My 141 g — — FDA listed —
American Red Cross 70% Isopropyl Alcohol 70 g/100g 51628-4526-01 MY 141 g — — FDA listed —
Isopro First Aid 70 mL/100mLthis 59898-0402-15 Water-Jel 24 bottles — — FDA listed —
Isopropyl Alcohol 70 mL/100mL 61010-5500-02 Safetec 59.1 ml — — FDA listed —
Isopropyl Alcohol .7 mL/mL 67777-0011-01 Dynarex 24 bottles — — FDA listed —
Isopropyl Alcohol 700 mL/L 69103-5500-00 Provision 0591 l — — FDA listed —
American Safety First Aid Antispetic 700 mg/1000mL 71927-0014-01 Orazen 59.1 ml — — FDA listed —
Isopropyl Alcohol 700 mL/L 73598-0651-01 JHK 0591 l — — FDA listed —
American Red Cross 70% Isopropyl Alcohol 70 g/100g 75742-0069-01 Zhejiang 141 g — — FDA listed —
MEDI-FIRST First Aid Antiseptic 70 mL/100mL 78495-0102-01 Ultra 59.1 ml — — FDA listed —
70% Isopropyl Alcohol 70 mL/100mL 83986-0810-17 UpLift 473 ml — — FDA listed —
Isopropyl Alcohol 700 mL/L 84269-3502-01 Wildman 0591 l — — 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

🏛️
2010
On the market since
May 2010
📍
2026
Currently FDA-listed
16 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
59898-0402-10 59 mL in 1 BOTTLE, SPRAY (59898-402-10) 2010-05-23 Active
59898-0402-15 You're viewing this 24 BOTTLE, SPRAY in 1 CASE (59898-402-15) / 59 mL in 1 BOTTLE, SPRAY (59898-402-10) 2010-05-23 Active

Pack size FAQ

What quantity is in NDC 59898-0402-15?
NDC 59898-0402-15 is listed by the FDA — 24 bottle, spray in 1 case / 59 ml in 1 bottle, spray.
What NDC number is used to bill for this package of Isopro First Aid Isopropyl Alcohol 70 mL/100mL Spray?
Bill NDC 59898-0402-15 — the 11-digit billing format is 59898040215. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 59898-402-15, 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: 59898-0402-15, written without dashes as 59898040215. 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 59898-0402-15, the first segment (59898) is the labeler code FDA assigned to Water-Jel Technologies; the middle segment (0402) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (15) 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 Water-Jel Technologies. 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 59 ml (59898-0402-10). 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?
Water-Jel Technologies 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 16 words ▾

Uses first aid to help decrease the risk of infection in minor cuts, scrapes and burns

⏱️ Dosage and Administration 32 words ▾

Directions clean the affected area spray a small amount of this product in the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

⚠️ Warnings 84 words ▾

For external use only Flammable keep away from fire or flame Do not use in the eyes or apply over large areas of the body longer than 1 week unless directed by a doctor Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns Stop use and consult a doctor if the condition persists or gets worse Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Isopropyl alcohol 70%

🧪 Inactive Ingredients 3 words ▾

Inactive ingredient water

🎯 Purpose 4 words ▾

Purpose First aid antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 59898-0401-10 · Water-Jel 59898-0403-10 · Water-Jel →
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.