Over-the-counter drug · OTC MONOGRAPH DRUG
Foaming Hand (Benzalkonium chloride) NDC 71897-224
Benzalkonium chloride 1.3 mg/mL · Soap · Topical · Veritiv Operating Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71897-224-86 | 7189702248671897022486 | 1000 mL in 1 BOTTLE, PLASTIC (71897-224-86)Marketed from Aug 1, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Foaming Hand
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Soap
- Route
- Topical
- Labeler
- Veritiv Operating CompanyNDC labeler code 71897
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 71897-224_4af5534d-3be0-730d-e063-6294a90a3eafSPL ID 4af5534d-3be0-730d-e063-6294a90a3eafSPL set ID 3b4dbfd0-f275-3502-e063-6294a90a8486RxCUI 1046593UNII F5UM2KM3W7
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471897022486followed by a unit qualifier and the quantityPackage 71897-0224-86. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses for handwashing to decrease bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 71897-224
- What is NDC 71897-224?
- 71897-224 is the product NDC for Foaming Hand (benzalkonium chloride), Benzalkonium chloride 1.3 mg/mL soap, listed with the FDA by Veritiv Operating Company. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Foaming Hand (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Veritiv Operating Company, NDC labeler code 71897. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Foaming Hand?
- 4 other product NDCs are listed under this name. See all Foaming Hand NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Foaming Hand products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Foaming Handbenzalkonium chloride | Benzalkonium chloride 1.3 mg/mL | SoapTopical | UpLift Brands, LLC | 83986-224 | 83986-0224-0883986-0224-4583986-0224-86 |
| Foaming Handfoaming hand soap | Cocoyl methyl monoethanolamine 1.2 g/100mL; Lauramidopropyl betaine 5 g/100mL | LiquidExtracorporeal | Zhejiang Meimi Technology Co., Ltd. | 41366-056 | 41366-0056-01 |
| Foaming Handbenzalkonium chloride | Benzalkonium chloride 1.3 mg/mL | LotionTopical | Cintas Corporation | 42961-224 | 42961-0224-71 |
| Foaming Handbenzalkonium chloride | Benzalkonium chloride 1.3 mg/mL | LotionTopical | Nice-Pak Products, LLC | 11344-224 | 11344-0224-0811344-0224-4511344-0224-86 |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
Showing 20 of 40.