Snugell Benzalkonium Chloride .13 g/100mL Spray, 473 mL
by QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD · 473 mL in 1 BOTTLE (80671-005-33)
NDC 80671-0005-33
🏷️ FDA NDC (as labeled)
80671-005-33
billing pads the product segment with a zero
OTC
Discontinued
Non-controlled
⚠ Inactivated by FDA
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0374-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
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
FDA NDC (as labeled)
80671-005-33
Product NDC
80671-005
11-digit billing NDC
80671000533
RxCUI
1039012
UNII
F5UM2KM3W7
UPC
0850057109337
Application #
505G(a)(3)
SPL Set ID
b4f6852c-5044-4ab9-8395-4ce8bf1d0a70
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Inactivated by FDA (certified through Dec 2026)
Marketing start
2022-03-18
Route
TOPICAL
Dosage form
SPRAY
Substance
BENZALKONIUM CHLORIDE
Why two NDCs?
The FDA registers this code as 80671-005-33 — 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 → 80671-0005-33. 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 Quaternary ammonium compounds class.
Drug family (ATC)
Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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.
🏭 Manufacturer & labeler
LabelerQUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code80671
First marketedMar 2022
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.
🩺 Clinical
🧪 What is this product?
Snugell Benzalkonium Chloride is an over-the-counter topical spray marketed under FDA's monograph rules for antiseptic and antimicrobial products. The active ingredient, benzalkonium chloride, functions as a broad-spectrum antimicrobial agent and is typically used in topical products to help reduce bacteria and germs on skin and minor wounds. This spray formulation allows for easy application to affected areas.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Benzalkonium Chloride — tap one for details:
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.
💬 Questions about Benzalkonium Chloride?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
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UNII 3XUS85K0RA
Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
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UNII G0R4UBI2ZZ
Matricaria chamomilla, commonly known as chamomile, is a plant extract used in medicines as a flavoring agent and natural fragrance component. It may also provide mild soothing properties to the formulation.
-
UNII C34U15ICXA
A plant extract from grape seeds that acts as an antioxidant and preservative in medications. It helps protect the active ingredients from degrading and extends the product's shelf life.
-
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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesAloe barbadensis leaf extract, butylene glycol, chamomilla recutita (matricaria) extract, grape seed extract, purified water.
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.
💲 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 system | Per mL | Per 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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Wound Wash Antiseptic Saline with Benzalkonium Chloride 1.3 mg/mL 13709-0235-11 | NeilMed | 75 ml | — | — | FDA listed | — |
| X3 Clean 1.3 mg/mL 26550-0002-10 | X3 | 8 ml | — | — | FDA listed | — |
| Lightning X Antiseptic 1.3 mg/100mL 43473-0303-01 | Nantong | 59.1 ml | — | — | FDA listed | — |
| Antiseptic 1.3 g/L 47682-0245-02 | Unifirst | 0591 l | — | — | FDA listed | — |
| Medi-First Antiseptic 1.3 g/L 47682-0254-02 | Unifirst | 0591 l | — | — | FDA listed | — |
| Antiseptic 1.3 g/L 47682-0316-02 | Unifirst | 0591 l | — | — | FDA listed | — |
| Green Guard Antiseptic 1.3 g/L 47682-0317-02 | Unifirst | 0591 l | — | — | FDA listed | — |
| Green Guard Antiseptic 1.3 g/L 47682-0333-02 | Unifirst | 0591 l | — | — | FDA listed | — |
| American Red Cross Antiseptic Cleansing 1.3 mg/mL 51628-0035-01 | MY | 177 ml | — | — | FDA listed | — |
| American Red Cross Antiseptic Cleansing .13 g/100mL 51628-4440-01 | MY | 177 ml | — | — | FDA listed | — |
| GenRx Hand Sanitizing 1.3 mg/mL 59088-0315-16 | PureTek | 237 ml | — | — | FDA listed | — |
| DiaSinc 1.3 mg/mL 59088-0596-16 | PureTek | 237 ml | — | — | FDA listed | — |
| First Aid Antiseptic .13 g/100mL 59898-0401-10 | Water-Jel | 59 ml | — | — | FDA listed | — |
| X3 Clean Hand Sanitizer 1.3 mg/mL 66902-0038-02 | Natural | 59 ml | — | — | FDA listed | — |
| Zoono Wound Cleanser .13 g/100mL 69221-0204-01 | Zoono | 50 ml | — | — | FDA listed | — |
| Antiseptic 1.3 g/L 69396-0153-02 | Trifecta | 0591 l | — | — | FDA listed | — |
| TOUCH Sanitizing Germ Block, Unscented, 1oz (28.35g) .13 g/100g 69744-0201-01 | Relevo, | 43 g | — | — | FDA listed | — |
| TOUCH Sanitizing Germ Block, Mint Green Tea Aloe, 1oz (28.35g) .13 g/100g 69744-0202-01 | Relevo, | 43 g | — | — | FDA listed | — |
| TOUCH Sanitizing Germ Block, Tropical Breeze, 1oz (28.35g) .13 g/100g 69744-0203-01 | Relevo, | 43 g | — | — | FDA listed | — |
| TOUCH Sanitizing Germ Block, Ocean Mist, 1oz (28.35g) .13 g/100g 69744-0204-01 | Relevo, | 43 g | — | — | FDA listed | — |
| ECOLAB Antiseptic 1.3 g/L 71338-0122-02 | ECOLAB | 059 l | — | — | FDA listed | — |
| My-Shield Hand Sanitizer .13 g/100mL 71884-0012-00 | Enviro | 10 ml | — | — | FDA listed | — |
| Germfree24 Hand Sanitizer .13 g/100mL 71884-0016-01 | Enviro | 10 ml | — | — | FDA listed | — |
| FIRST SHIELD First Aid Antiseptic .13 g/100mL 72976-0003-01 | Ever | 60 ml | — | — | FDA listed | — |
| American Red Cross Antiseptic Cleansing .13 g/100mL 75742-0037-01 | Zhejiang | 177 ml | — | — | FDA listed | — |
| MEDI-FIRST First Aid Antiseptic 1.3 mg/mL 78495-0122-01 | Ultra | 59.1 ml | — | — | FDA listed | — |
| Snugell .13 g/100mLthis 80671-0005-33 | QUANZHOU | 473 ml | — | — | Discontinued | — |
| Xtra .13 g/100mL 51628-4439-01 | MY | 399 ml | — | — | FDA listed | — |
| Xtra .13 g/100mL 84987-0001-01 | Zhejiang | 399 ml | — | — | FDA listed | — |
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
🏛️
2022
On the market since
Mar 2022
📍
2026
Currently FDA-listed
4 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 80671-0005-33 You're viewing this | 473 mL in 1 BOTTLE (80671-005-33) | 2022-03-18 | Inactivated by FDA |
🧭 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 FDA registers it as 80671-005-33, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 80671-0005-33, written without dashes as 80671000533. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 80671-0005-33, the first segment (80671) is the labeler code FDA assigned to QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD; the middle segment (0005) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (33) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
QUANZHOU AIWINA HYGIENE PRODUCTS CO.,LTD 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.
📄 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
📦 Storage and Handling
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
⏱️ Dosage and Administration ▾
Directions • Spray onto your CPAP cushion or CPAP machine and then gently wipe with a paper towel or a soft towel to clean. • Children under 6 years of age should be supervised when using this product.
⚠️ Warnings ▾
Warnings For external use only. Do Not Use • On children less than 2 months of age • Near eyes or on open skin wounds When using this product avoid contacting with eyes. In case of eye contact, rinse eyes with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away at 800-222-1222.
📦 Storage and Handling ▾
Other Information • Avoid freezing and store below 110F (43C). • Dispose of the empty can in a recycling bin.
🧪 Active Ingredient ▾
Active Ingredient Benzalkonium Chloride 0.13% (w/w)
🧪 Inactive Ingredients ▾
Inactive Ingredients Aloe barbadensis leaf extract, butylene glycol, chamomilla recutita (matricaria) extract, grape seed extract, purified water.
🎯 Purpose ▾
Purpose Antiseptic
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.