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Quality Choice Eye Wash Water 99.05 g/100mL Solution/ Drops — NDC 83324-0192-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Quality Choice Eye Wash Water 99.05 g/100mL Solution/ Drops — NDC 83324-192-04 (Billing 83324-0192-04)

by Chain Drug Marketing Assoc., Inc. · 1 BOTTLE, WITH APPLICATOR in 1 BOX / 118 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of Quality Choice Eye Wash Water 99.05 g/100mL Solution/ Drops from Chain Drug Marketing Assoc., Inc., marketed since Aug 2024 and currently FDA-listed; retail pharmacies pay about $0.0288 per mL (NADAC). It is this product's only package size.

NDC 83324-0192-04
🏷️ FDA NDC (as labeled) 83324-192-04 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 Water (different manufacturers) — 3 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 2, 2026 — Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. (B BRAUN MEDICAL INC) · FDA recall D-0495-2026
Class II · Dec 22, 2025 — Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution (Baxter Healthcare Corporation) · FDA recall D-0296-2026
Class II · Aug 26, 2025 — Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment. (B BRAUN MEDICAL INC) · FDA recall D-0652-2025
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) 83324-192-04
Product NDC 83324-192
11-digit billing NDC 83324019204
RxCUI 1053429
UNII 059QF0KO0R
UPC 0635515997936
Application # M018
SPL Set ID 1fb8a109-351b-7039-e063-6394a90a7311
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-08-15
Route OPHTHALMIC
Dosage form SOLUTION/ DROPS
Substance WATER

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

GCN Seq No 039494
GCN 95766
HICL code 018251
Ingredient (HICL) Sod Borate/Boric Ac/Water/Nacl
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q6
Therapeutic class — intermediate (HIC2) Ophthalmic Preparations
HIC3 code Q6E
Therapeutic class — specific (HIC3) Eye Irrigations
AHFS code 52:92.00.00
AHFS class Eent Drugs, Miscellaneous
FDB label name QC EYE WASH IRRIGATING SOLN
FDB brand name Eye Wash
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 039494
  • GCN: 95766
  • HICL (First Databank): 018251
  • AHFS class code: 52:92.00.00
  • RxCUI (RxNorm): 1053429
Why two NDCs? The FDA registers this code as 83324-192-04 — 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 → 83324-0192-04. 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.

Clinical

Label name QC EYE WASH IRRIGATING SOLN Ingredient Sod Borate/Boric Ac/Water/Nacl
📗 Our plain-language guide HelloPharmacist
  • It can seem a little odd at first. In these products, sterile water plays the essential role of carrying or dissolving the actual active medication — like insulin — so it can be sa...
  • Why is 'water' listed as the active ingredient on my medicine?
  • No — these are very different products that should never be used interchangeably. Sterile Water for Injection is used only as a diluent for other drugs given by needle, and it must...
  • Is Sterile Water for Injection the same as the eye wash or the irrigation product?
📖 Read our full Water 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 mLPer package
Retail pharmacies payNADAC · weekly $0.029 $3.40 / 118 ml
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.
NADAC price history (per mL) — tap or hover for the price & month
Dec 2025 Mar 2026 Jun 2026 Sep 2026 $0.030 $0.022
▲ Up 31% over the last 10 months.
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
83324-0192-04 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 BOX / 118 mL in 1 BOTTLE, WITH APPLICATOR 2024-08-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rugby Eye Wash 99.05 g/100mL 00536-1224-97 Rugby 1 bottle $0.029 — Availability likely —
Leader Eye Wash 99.05 g/100mL 70000-0018-01 Cardinal 1 bottle $0.029 — Availability likely —
Quality Choice Eye Wash 99.05 g/100mLthis 83324-0192-04 Chain 1 bottle $0.029 — Availability likely —
Walgreens Sterile Soothing Eye Wash 99.05 mL/100mL 00363-0700-04 Walgreens 1 bottle — — FDA listed —
Rite Aid Eye Wash 99.05 g/100mL 11822-2313-01 Rite 1 bottle — — FDA listed —
Eye Wash 99.05 mL/100mL 11822-9860-08 Rite 1 bottle — — Discontinued —
Advanced Eye Relief Eye Wash 99.05 mL/100mL 24208-0005-04 Bausch 1 applicator — — FDA listed —
Eye Wash 99.05 mL/100mL 30142-0010-18 Kroger 1 bottle — — FDA listed —
Eye Wash 991 mg/mL 49687-0010-01 CMC 1 tube — — FDA listed —
Rugby Eye Wash 99.05 g/100mL 50090-7440-00 A-S 1 bottle — — FDA listed —
Medics Choice Soothing Eye Wash 99.05 g/100mL 55651-0555-01 KC 118 ml — — FDA listed —
Eye Wash 99.05 mL/100mL 59779-0337-09 CVS 1 bottle — — FDA listed —
Plus Rinse Emergency Eyewash 99.1 mL/100mL 72598-0022-20 INNOVATIVE 500 ml — — FDA listed —
Eye Wash 991 mg/mL 82001-0001-00 Jiangxi 30 ml — — FDA listed —
Eye Wash 991 mg/mL 82996-0007-01 Hubei 15 ml — — FDA listed —
Eye Wash 99.1 mL/100mL 84219-0007-15 M-star 15 ml — — FDA listed —
Huanggang Eye Wash 99 mL/100mL 85426-0002-01 Huanggang 15 ml — — Discontinued —
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
Aug 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 F5UM2KM3W7
    Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
  • UNII R57ZHV85D4
    Boric acid is a weak acid derived from boron. In medicines, it typically serves as a buffer to help maintain the product's pH level and may act as a preservative in certain formulations.
  • UNII 91MBZ8H3QO
    Sodium borate is an inorganic salt compound used in medicines as a buffer to help maintain a stable pH level, and sometimes as a mild preservative or cleansing agent in topical formulations.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.

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

The official label also statesboric acid, sodium borate and sodium chloride. PRESERVATIVE ADDED: benzalkonium chloride (0.01%)

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

LabelerChain Drug Marketing Assoc., Inc.
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code83324
First marketedAug 2024
Product typeHuman Otc Drug
Portfolio4 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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 24 words ▾

Uses washes the eye to help relieve irritation discomfort burning stinging itching by removing loose foreign material air pollutants (smog or pollen) chlorinated water

⏱️ Dosage and Administration 106 words ▾

Directions For use with nozzle applicator. flush the affected eye(s) as needed control the rate of flow of solution by pressure on the bottle do not touch dropper tip to eye When using an eye cup rinse the cup with Eye Wash immediately before each use avoid contamination of the rim and inside surfaces of the cup fill the cup half full with Eye Wash Solution and apply the cup to the affected eye(s), pressing tightly to prevent spillage tilt the head backward. Open eyelids wide and rotate eyeball to thoroughly wash the eye rinse cup with clean water after each use replace cap after use

⚠️ Warnings 100 words ▾

Warnings For external use only Do not use if you have open wounds in or near the eyes, and get medical help right away if solution changes color or becomes cloudy When using this product remove contact lenses before using do not touch tip of container to any surface to avoid contamination replace cap after use Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye condition worsens or persists Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Purified water (99.05%)

🧪 Inactive Ingredients 14 words ▾

Inactive ingredients boric acid, sodium borate and sodium chloride. PRESERVATIVE ADDED: benzalkonium chloride (0.01%)

🎯 Purpose 2 words ▾

Purpose Eyewash

📄 Do Not Use 26 words ▾

Do not use if you have open wounds in or near the eyes, and get medical help right away if solution changes color or becomes cloudy

📄 When Using This Product 25 words ▾

When using this product remove contact lenses before using do not touch tip of container to any surface to avoid contamination replace cap after use

📄 Stop Use and Ask a Doctor If 25 words ▾

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye condition worsens or persists

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 31 words ▾

Other information store at 15º-25ºC (59º-77ºF) keep tightly closed does not contain thimerosal enclosed eyecup is sterile if packaging is intact use before expiration date marked on the carton or bottle

📄 Package Label / Principal Display Panel 12 words ▾

Quality Choice Eye Wash 118 mL Quality Choice Eye Wash 118 mL

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 Quality Choice Eye Wash (this brand).

Top reported reactions

Fatigue39
Pain34
Dyspnoea32
Nausea32
Vomiting26
Diarrhoea25
Malaise25

Reporter sex

573 reports
Male · 38%
Female · 62%
Unknown · 0%

Serious outcomes

Hospitalization156
Life-threatening32
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 80 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.
← 83324-0191-14 · Chain 83324-0194-50 · Chain →
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.