Home › NDC Lookup › Ingredients › Water, Purified › 50090-7440-00
RUGBY EYE WASH Water, purified 99.05 g/100mL Solution — NDC 50090-7440-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

RUGBY EYE WASH Water, purified 99.05 g/100mL Solution — NDC 50090-7440-0 (Billing 50090-7440-00)

by A-S Medication Solutions · 1 BOTTLE, DROPPER in 1 BOX / 118 mL in 1 BOTTLE, DROPPER

This is a package of RUGBY EYE WASH Water, purified 99.05 g/100mL Solution from A-S Medication Solutions, marketed since Feb 2019 and currently FDA-listed. It is this product's only package size.

NDC 50090-7440-00
🏷️ FDA NDC (as labeled) 50090-7440-0 billing pads the package 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

NDC database record

One package, one record: these facts belong to NDC 50090-7440-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
50090 labeler · 7440 product · 0 package
Package marketed since
Nov 6, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5009074400 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 50090-7440-0
Product NDC 50090-7440
11-digit billing NDC 50090744000
NCPDP billing unit ML — per mL (volume)
RxCUI 1053429
UNII 059QF0KO0R
Application # M018
SPL Set ID 0773e558-2f46-494c-888a-3bc517202b65
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-02-22
Route OPHTHALMIC
Dosage form SOLUTION
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 EYE WASH SOLUTION
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 50090-7440-0 — a 5-4-1 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 package segment → 50090-7440-00. 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 EYE WASH SOLUTION 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 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
50090-7440-00 You're viewing this Main listing 1 BOTTLE, DROPPER in 1 BOX / 118 mL in 1 BOTTLE, DROPPER 2024-11-06 — 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/100mL 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/100mLthis 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

🏛️
2019
On the market since
Feb 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.

💡 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

LabelerA-S Medication Solutions
FDA applicationM018 (OTC MONOGRAPH DRUG)
Labeler code50090
First marketedFeb 2019
Product typeHuman Otc Drug
Portfolio2,811 products on file

More NDCs from A-S Medication Solutions labeler code 50090

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 📦 How Supplied / Storage and Handling 🧪 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 📄 Questions or Comments 📄 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 107 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 Solution 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 105 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 the tip of container to any surface to avoid contamination replace cap after each 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 (1-800-222-1222) right away.

📦 How Supplied / Storage and Handling 17 words ▾

HOW SUPPLIED Product: 50090-7440 NDC: 50090-7440-0 118 mL in a BOTTLE, DROPPER / 1 in a BOX

🧪 Active Ingredient 5 words ▾

Active ingredients 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 27 words ▾

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

📄 Stop Use and Ask a Doctor If 27 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 20 words ▾

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

📄 Other Information 31 words ▾

Other information Store at 15°-25°C (59°-77°F) 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

📄 Questions or Comments 22 words ▾

Questions or Comments? Toll free product Information or to report a Serious Side Effect Associated with use of this product Call: 1-800-645-2158

📄 Package Label / Principal Display Panel 4 words ▾

Water, purified Label Image

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 A-S Medication Solutions. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
A-S Medication Solutions 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.
← 50090-7439-02 · A-S 50090-7441-00 · A-S →
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.