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Green Guard First Aid Eye Wash Water .983 mg/mL Solution, 946 mL — NDC 47682-0412-26 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Green Guard First Aid Eye Wash Water .983 mg/mL Solution, 946 mL — NDC 47682-412-26 (Billing 47682-0412-26)

by Unifirst First Aid Corporation · 946 mL in 1 BOTTLE, DISPENSING

This is a package of 946 mL of Green Guard First Aid Eye Wash Water .983 mg/mL Solution from Unifirst First Aid Corporation, marketed since Oct 2015 and currently FDA-listed.

NDC 47682-0412-26
🏷️ FDA NDC (as labeled) 47682-412-26 billing pads the product segment with a zero
This package
Contains946 mL Pack sizes2 compare ↓
Product page 47682-0412-11 Also comes in: 473 ml 47682-412-11
OTC Brand 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 47682-412-26 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
47682 labeler · 412 product · 26 package
Package marketed since
Apr 1, 2016
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4768241226 5
FDA record last changed
Jul 24, 2026
⚠️
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) 47682-412-26
Product NDC 47682-412
11-digit billing NDC 47682041226
RxCUI 1151101
UNII 059QF0KO0R
Application # NDA022305
SPL Set ID a4ba5526-b4e2-4bcc-9127-aa22ebf5017f
DEA schedule Non-controlled
Marketing category NDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-10-01
Route OPHTHALMIC
Dosage form SOLUTION
Substance WATER
Quick answers
  • RxCUI (RxNorm): 1151101
Why two NDCs? The FDA registers this code as 47682-412-26 — 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 → 47682-0412-26. 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

📗 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.
Try another pack size: 473 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
47682-0412-11 47682-412-11 Main listing 473 mL in 1 BOTTLE, DISPENSING 2015-10-01 — Active
47682-0412-26 You're viewing this 946 mL in 1 BOTTLE, DISPENSING 2016-04-01 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 946 mL — 946 ml in 1 bottle, dispensing.
How does this package differ from NDC 47682-0412-11?
Both are Green Guard First Aid Eye Wash Water .983 mg/mL Solution — the drug itself is identical. This page's package is the 946 mL one, while NDC 47682-0412-11 is the 473 ml package.
What NDC number is used to bill for this package of Green Guard First Aid Eye Wash Water .983 mg/mL Solution?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PhysiciansCare Ophthalmic Solution Eyewash Purified Water, 98.3% 465 mL/473mL 00924-0158-16 Acme 473 ml — — FDA listed —
PhysiciansCare Ophthalmic Solution Eyewash 929 g/946mL 00924-0160-01 Acme 30 ml — — FDA listed —
PhysiciansCare Ophthalmic Solution Eyewash 929 g/946mL 00924-0162-08 Acme 236 ml — — FDA listed —
Physicians Care Eyewash 465 mL/473mL 00924-0163-01 Acme 29 ml — — FDA listed —
Easy Care First Aid Eyewash 929 g/946mL 44224-0160-01 Tender 30 ml — — FDA listed —
Medi-First First Aid Eye Wash 983 mg/mL 47682-0197-11 Unifirst 473 ml — — FDA listed —
Medi-First First Aid Eye Wash 983 mg/mL 47682-0198-08 Unifirst 236 ml — — FDA listed —
Green Guard First Aid Eye Wash .983 mg/mL 47682-0410-08 Unifirst 236 ml — — FDA listed —
Green Guard First Aid Eye Wash .983 mg/mLthis 47682-0412-26 Unifirst 946 ml — — FDA listed —
Medi-First Plus First Aid Eye Wash .983 mg/mL 47682-0936-18 Unifirst 118 ml — — FDA listed —
Eye Clean 98.3 mL/100mL 50332-0201-01 HART 118 ml — — FDA listed —
AeroWash Eyewash .983 mL/mL 55305-0115-10 Aero 30 ml — — FDA listed —
ULINE Eyewash 465 mL/473mL 65785-0125-01 Niagara 473 ml — — FDA listed —
Pur-Wash 929 g/946mL 65785-0160-01 Niagara 30 ml — — FDA listed —
Pur-Wash 929 g/946mL 65785-0162-01 Niagara 236 ml — — Discontinued —
Pur-Wash 929 g/946mL 65785-0166-01 Niagara 473 ml — — FDA listed —
Pur-Wash 465 mL/473mL 65785-0168-01 Niagara 473 ml — — FDA listed —
Pur-Wash 929 g/946mL 65785-0169-01 Niagara 30 ml — — FDA listed —
Eye wash 98.3 mL/100mL 68599-1981-01 McKesson 29.6 ml — — FDA listed —
ULINE Eyewash 465 mL/473mL 69790-0010-16 Uline. 473 ml — — FDA listed —
Firstep Firstflush 465 mL/473mL 70290-0310-32 Encon 946 ml — — FDA listed —
ECOLAB Eye Wash .983 mg/mL 71338-0119-18 ECOLAB 118 ml — — FDA listed —
Dynamic Eyewash with Eyecup 929 g/946mL 72745-0101-16 Dynamic 473 ml — — FDA listed —
Kollourion Eyesalve Eyewash 929 g/946mL 72924-0001-01 Miracle 1 bottle — — FDA listed —
Thompson Safety Eyewash 929 g/946mL 73408-0198-18 Thompson 118 ml — — FDA listed —
Crane Safety Eye Wash .983 mg/mL 73408-0936-18 Crane 118 ml — — FDA listed —
Eyewash 465 mL/473mL 78641-0786-67 Global 473 ml — — FDA listed —
About this product: this is the brand-name version. We did not find an FDA-approved generic match for this exact strength, form and route.
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

🏛️
2015
On the market since
Oct 2015
📍
2026
Currently FDA-listed
11 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.

🧪 Avoiding an ingredient? See Water inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

  • 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.

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

The official label also statesInactive ingredients boric acid, sodium borate, sodium chloride

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

LabelerUnifirst First Aid Corporation
Application holderNIAGARA PHARMACEUTICALS INC
FDA applicationNDA022305 (NDA)
Labeler code47682
First marketedOct 2015
Product typeHuman Otc Drug
Portfolio183 products on file

More NDCs from Unifirst First Aid Corporation labeler code 47682

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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Use For cleansing the eye to help relieve irritation or burning by removing loose foreign material.

⏱️ Dosage and Administration 19 words ▾

Directions Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 5 words ▾

Active ingredient Purified water 98.3%

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients boric acid, sodium borate, sodium chloride

🎯 Purpose 2 words ▾

Purpose Eyewash

📄 Do Not Use 26 words ▾

Do not use if you experience any open wounds in or near the eyes and obtain immediate medical treatment if solution changes color or becomes cloudy

📄 When Using This Product 22 words ▾

When using this product to avoid contamination, do not touch tip of container to any surface do not reuse once opened, discard

📄 Stop Use and Ask a Doctor If 25 words ▾

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

📄 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 52 words ▾

Other information lot number is printed on the bottle store at 20º to 25º C [68º to 77º F) for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL” do not use if this seal is missing or broken use before expiration date marked on bottle

📄 Questions or Comments 3 words ▾

Questions? Call 800-869-6970

📄 Package Label / Principal Display Panel 85 words ▾

Green Guard Eye Wash Label Sterile and Isotonic Eye Wash solution NDC 47682-410-70 Purified water 98.3% Cleanses the eye by removing loose foreign material Green Guard® 4 - 1 fl oz (30 mL) Bottles Order# 4110P Green Guard

Green Guard Eye Wash Label First Aid eye wash Purified Water, 98.3% Ophthalmic Solution Eyewash NDC 47682-412-11 Single Use Green Guard® 3499 Rider Trail South St. Louis, MO 63045 Made in Canada Product # 4107 Sterile Solution 16 fl oz [473 mL] 3 47682 04107 6 4107

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

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 Unifirst First Aid Corporation. 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 473 ml (47682-0412-11). 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?
Unifirst First Aid Corporation 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.
← 47682-0410-08 · Unifirst 47682-0432-46 · Unifirst →
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.