Zoono Hand Sanitizer benzalkonium chloride .13 g/100mL Solution, 1000 mL — NDC 69221-203-15 (Billing 69221-0203-15)
This is a package of 1,000 mL of Zoono Hand Sanitizer benzalkonium chloride .13 g/100mL Solution from Zoono Holdings USA, marketed since Nov 2020 and currently FDA-listed, this package's marketing is listed to end Dec 2026.
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1049254
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Quaternary ammonium compounds class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Zoono Hand Sanitizer is a topical solution containing benzalkonium chloride, an antimicrobial agent commonly used in over-the-counter hand sanitizers and topical antiseptic products. This product is marketed under FDA's OTC monograph rules for antiseptic hand-sanitizing agents. Benzalkonium chloride is typically used to help reduce bacteria on the skin. The solution is applied directly to the hands as a liquid sanitizer.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Benzalkonium Chloride — tap one for details:
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 3, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 69221-0203-11 69221-203-11 Main listing | 50 mL in 1 BOTTLE | 2020-11-20 | Dec 31, 2026 | Active |
| 69221-0203-13 69221-203-13 | 150 mL in 1 BOTTLE | 2020-11-20 | Dec 31, 2026 | Active |
| 69221-0203-14 69221-203-14 | 500 mL in 1 BOTTLE | 2020-11-20 | Dec 31, 2026 | Active |
| 69221-0203-15 You're viewing this | 1000 mL in 1 BOTTLE | 2020-11-20 | Dec 31, 2026 | Active |
| 69221-0203-16 69221-203-16 | 3785 mL in 1 BOTTLE | 2020-11-20 | Dec 31, 2026 | Active |
You're viewing one of 5 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 69221-0203-11?
What NDC number is used to bill for this package of Zoono Hand Sanitizer benzalkonium chloride .13 g/100mL Solution?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Sep 3, 2026
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.
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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.
1 inactive ingredient listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Directions: Apply liberally to hands and gently rub until dry.
⏱️ Dosage and Administration ▾
Uses: For Personal hand sanitizing and to reduce bacteria on the skin. Recommended for repeated use.
⚠️ Warnings ▾
Warnings: For external use only. Do not use in the eyes When using this product avoid contact with eyes. In case of eye contact flush eyes with water. Stop use and ask a doctor if irritation and redness develops. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Do not use in the eyes When using this product avoid contact with eyes. In case of eye contact flush eyes with water.
🧪 Active Ingredient ▾
Active Ingredient Benzalkonium Chloride 0.13% Purpose: Antiseptic
🧪 Inactive Ingredients ▾
Inactive Ingredients: Ethyl alcohol, Fragrances, Silica Complex (3-Trimethoxysilyl Propyl Dimethyl Octadecyl Ammonium Chloride), Water
🎯 Purpose ▾
Purpose: Antiseptic
📄 Ask a Doctor Before Use If ▾
Stop use and ask a doctor if irritation and redness develops.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions? Telephone 1-844-966-6687 Monday through Friday 8:00am till 5:00pm EST
📄 Package Label / Principal Display Panel ▾
typical
About this NDC listing & data coverage
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. |