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DURMA DynaWound Cleanser Wound .13 g/100mL Spray, 12 bottles — NDC 67777-0403-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

DURMA DynaWound Cleanser Wound .13 g/100mL Spray, 12 bottles — NDC 67777-403-04 (Billing 67777-0403-04)

by Dynarex Corporation · 12 BOTTLE in 1 CASE / 118.3 mL in 1 BOTTLE

This is a package of 12 bottles of DURMA DynaWound Cleanser Wound .13 g/100mL Spray from Dynarex Corporation, marketed since Feb 2017 and currently FDA-listed.

NDC 67777-0403-04
🏷️ FDA NDC (as labeled) 67777-403-04 billing pads the product segment with a zero
This package
Contains12 bottles Pack sizes2 compare ↓
Product page 67777-0403-02 Also comes in: 24 bottles 67777-403-02
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 67777-403-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
67777 labeler · 403 product · 04 package
Package marketed since
Mar 30, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0616784300511, 0840117346628
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 67777-403-04
Product NDC 67777-403
11-digit billing NDC 67777040304
RxCUI 582205
UNII PH41D05744
UPC 0616784300511, 0840117346628
Application # M003
SPL Set ID 6a4dd82a-6b06-426b-9afd-415a1a4339b4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-02-13
Route TOPICAL
Dosage form SPRAY
Substance BENZETHONIUM CHLORIDE

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

GCN Seq No 053936
GCN 21725
HICL code 004259
Ingredient (HICL) Benzethonium Chloride
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5B
Therapeutic class — specific (HIC3) Topical Preparations,Antibacterials
AHFS code 84:04.92.00
AHFS class Local Anti-Infectives, Miscellaneous
FDB label name DYNAWOUND CLEANSER
FDB brand name Dynawound
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 053936
  • GCN: 21725
  • HICL (First Databank): 004259
  • AHFS class code: 84:04.92.00
  • RxCUI (RxNorm): 582205
Why two NDCs? The FDA registers this code as 67777-403-04 — 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 → 67777-0403-04. 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.

RxNorm drug class

This medicine belongs to the Antiseptics class.

Drug family (ATC) Antiseptics, Quaternary ammonium compounds
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

Label name DYNAWOUND CLEANSER Ingredient Benzethonium Chloride
🧪 What is this product?

This is a topical wound spray containing benzethonium chloride, an antimicrobial agent that is typically used to help cleanse and disinfect minor wounds and cuts. As an over-the-counter monograph product, it is marketed under FDA's established rules for this category of antiseptic skin cleaners rather than through individual product approval. The spray form allows for direct application to the affected area.

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: 24 bottles
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
67777-0403-02 67777-403-02 Main listing 24 BOTTLE, SPRAY in 1 CASE / 236.5 mL in 1 BOTTLE, SPRAY 2017-02-13 — Active
67777-0403-04 You're viewing this 12 BOTTLE in 1 CASE / 118.3 mL in 1 BOTTLE 2026-03-30 — Active

Pack size FAQ

What quantity is in this package?
This package contains 12 bottles — 12 bottle in 1 case / 118.3 ml in 1 bottle.
How does this package differ from NDC 67777-0403-02?
Both are DURMA DynaWound Cleanser Wound .13 g/100mL Spray — the drug itself is identical. This page's package is the 12 bottles one, while NDC 67777-0403-02 is the 24 bottles package.
What NDC number is used to bill for this package of DURMA DynaWound Cleanser Wound .13 g/100mL Spray?
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
Walgreens Antiseptic Wound Wash 1.3 mg/g 00363-1507-41 Walgreen 211 g — — FDA listed —
Antiseptic Wound Care MediCleanse Healing 1.3 mg/g 42829-0002-21 ASCENT 211 g — — FDA listed —
ProCure Antiseptic Wound Cleanser .13 g/100mL 55681-0052-08 Twin 236 ml — — FDA listed —
DURMA DynaWound Cleanser .13 g/100mLthis 67777-0403-04 Dynarex 12 bottles — — FDA listed —
Dermal Wound Cleanser 1.3 g/981mL 69740-0490-00 Smith 473 ml — — FDA listed —
Dermal Wound Cleanser 1.3 g/981mL 69740-0492-00 Smith 236 ml — — FDA listed —
CVS Antiseptic Wound Wash 1.3 mg/g 69842-0327-21 CVS 211 g — — FDA listed —
Sterile Antibacterial Wound Wash 1.3 mg/mL 71029-0390-04 Cosrich 120 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

🏛️
2017
On the market since
Feb 2017
📍
2026
Currently FDA-listed
9 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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

LabelerDynarex Corporation
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code67777
First marketedFeb 2017
Product typeHuman Otc Drug
Portfolio60 products on file

More NDCs from Dynarex Corporation labeler code 67777

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 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use(s) First aid to help prevent infection in minor cuts, scrapes, and burns

⏱️ Dosage and Administration 36 words ▾

Directions • Clean the affected area • Spray a small amount of this product on the area 1 to 3 times daily • May be covered with a sterile bandage • If bandaged let dry first

⚠️ Warnings 79 words ▾

Warnings For External Use Only Do not use • In the eyes or 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 ask a doctor if if condition persists or gets worse. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzethonium Chloride 0.13%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Benzyl Alcohol, Disodium Edetate, Glycerin, Polyquaternium 10, Polysorbate 20, Purified Water, Sodium Citrate.

🎯 Purpose 4 words ▾

Purpose First Aid Antibiotic

📄 Do Not Use 24 words ▾

Do not use • In the eyes or over large areas of the body • Longer than 1 week unless directed by a doctor

📄 Ask a Doctor Before Use If 17 words ▾

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if if condition persists or gets worse.

📄 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 13 words ▾

Other Information • Store at room temperature 15°-30ºC (59º-86ºF) • Avoid excessive heat

📄 Package Label / Principal Display Panel 10 words ▾

Label Durma DynaWound Cleanser 3005 IN MASTER

Label 3004 3004_IN_MASTER

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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Dynarex 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 24 bottles (67777-0403-02). 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?
Dynarex 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.
← 67777-0402-02 · Dynarex 67777-0405-02 · Dynarex →
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.