Over-the-counter drug · OTC MONOGRAPH DRUG
Foaming Sanitizing Hand (Benzalkonium chloride) NDC 50865-683
Benzalkonium chloride .003 mg/mL · Soap · Topical · Kutol Products Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50865-683-04 | 5086506830450865068304 | 1000 mL in 1 BAG (50865-683-04)Marketed from Jun 12, 2017 | |
| 50865-683-17 | 5086506831750865068317 | 50 mL in 1 BOTTLE, PLASTIC (50865-683-17)Marketed from Jun 12, 2016 | |
| 50865-683-41 | 5086506834150865068341 | 1000 mL in 1 BAG (50865-683-41)Marketed from Oct 1, 2015 | |
| 50865-683-44 | 5086506834450865068344 | 1000 mL in 1 BAG (50865-683-44)Marketed from Jun 12, 2016 |
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 Sanitizing Hand
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — .003 mg/mL
- Dosage form
- Soap
- Route
- Topical
- Labeler
- Kutol Products CompanyNDC labeler code 50865
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 50865-683_298dd564-db49-47a0-e063-6394a90ac4c3SPL ID 298dd564-db49-47a0-e063-6394a90ac4c3SPL set ID 95f0af0e-7889-4c2a-9573-4242acfd6684UNII F5UM2KM3W7UPC 0686702683095
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
N450865068304followed by a unit qualifier and the quantityPackage 50865-0683-04. 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 skin
Excerpt only. Read the full label for complete information.
About NDC 50865-683
- What is NDC 50865-683?
- 50865-683 is the product NDC for Foaming Sanitizing Hand (benzalkonium chloride), Benzalkonium chloride .003 mg/mL soap, listed with the FDA by Kutol Products Company. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Foaming Sanitizing Hand (Benzalkonium chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Kutol Products Company, NDC labeler code 50865. 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 Sanitizing Hand?
- 1 other product NDC are listed under this name. See all Foaming Sanitizing 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 Sanitizing 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 Sanitizing Handalcohol | Alcohol .072 mg/mL | SoapTopical | Kutol Products Company | 50865-710 | 50865-0710-1750865-0710-4150865-0710-44+3 more |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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