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Sterile Antibacterial Wound Wash Benzethonium Chloride 1.3 mg/mL Spray, 120 mL — NDC 71029-0390-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Sterile Antibacterial Wound Wash Benzethonium Chloride 1.3 mg/mL Spray, 120 mL — NDC 71029-390-04 (Billing 71029-0390-04)

by Cosrich Group, Inc. · 120 mL in 1 CAN

This is a package of 120 mL of Sterile Antibacterial Wound Wash Benzethonium Chloride 1.3 mg/mL Spray from Cosrich Group, Inc., no longer marketed (first marketed May 2017), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 71029-0390-04
🏷️ FDA NDC (as labeled) 71029-390-04 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 71029-390-04 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71029 labeler · 390 product · 04 package
Package marketed since
May 9, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7102939004 6
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71029-390-04
Product NDC 71029-390
11-digit billing NDC 71029039004
RxCUI 582205
UNII PH41D05744
Application # M003
SPL Set ID d86d3988-ee4b-4396-8b5a-164c4f0394e6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2017-05-09
Route TOPICAL
Dosage form SPRAY
Substance BENZETHONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 582205
Why two NDCs? The FDA registers this code as 71029-390-04 — 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 → 71029-0390-04. 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

🧪 What is this product?

This is a topical spray wound cleanser containing benzethonium chloride, an antibacterial agent. It is an over-the-counter monograph product marketed to help cleanse minor wounds and skin irritations by reducing bacteria on the affected area. The spray form allows for direct application to the wound site. Benzethonium chloride is commonly used in first-aid and wound-care products as a topical antiseptic.

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
71029-0390-04 You're viewing this Main listing 120 mL in 1 CAN 2017-05-09 — Inactivated by FDA

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/100mL 67777-0403-02 Dynarex 24 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/mLthis 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
May 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.

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

  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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 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.
  • 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.

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

The official label also statesAloe Barbadensis Leaf Extract, benzalkonium chloride, Purified Water, Sodium Chloride U.S.P.

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

LabelerCosrich Group, Inc.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code71029
First marketedMay 2017
Product typeHuman Otc Drug
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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 17 words ▾

Uses first aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

⏱️ Dosage and Administration 39 words ▾

Directions clean the affected area shake well remove seal and cap spray a small amount of this product on the area 1 to 3 times a day may be covered with a sterile bandage. If bandaged, let dry first

⚠️ Warnings 73 words ▾

Warnings For external use only Do not use in eyes over large areas of the body longer than 1 week unless directed by a doctor Ask a doctor before use in the event of deep puncture wounds, animal bites or severe burns Stop use and ask a doctor if condition persists or gets worse Keep out of reach of childrens If swallowed get medical help or contact a Poison Control Center right away

🧪 Active Ingredient 5 words ▾

Active ingredients Benzethonium Chloride 0.13%

🧪 Inactive Ingredients 13 words ▾

Inactive ingredients Aloe Barbadensis Leaf Extract, benzalkonium chloride, Purified Water, Sodium Chloride U.S.P.

🎯 Purpose 4 words ▾

Purpose First Aid Antiseptic

📄 Do Not Use 20 words ▾

Do not use in eyes 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 in the event of deep puncture wounds, animal bites or severe burns

📄 Stop Use and Ask a Doctor If 12 words ▾

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

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Questions or Comments 2 words ▾

Questions? 1-800-831-7210

📄 Package Label / Principal Display Panel 54 words ▾

Principal Display Panel NDC 71029-390-04 PRO+ECT Antibacterial WOUND WASH FIRST AID CLEANSER Cleans wounds painlessly and effectively No burn or sting No alcohol No fragrance ECO-FRIENDLY No Fluorinated Hydrocarbon Propellants COMPRESSED AIR IS THE PROPELLANT SPRAYS UPSIDE DOWN OR AT ANY ANGLE NO PUMPING NEEDED 360 0 CONTINUOUS SPRAY 4 FL.OZ (120 mL) Label

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
Cosrich Group, Inc. 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.
← 71028-9111-01 · SUNJIN 71034-0001-60 · Xiamen →
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.