Over-the-counter drug · OTC MONOGRAPH DRUG
Foaming Sanitizing Hand (Alcohol) NDC 50865-710
Alcohol .072 mg/mL · Soap · Topical · Kutol Products Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50865-710-17 | 5086507101750865071017 | 50 mL in 1 BOTTLE, PLASTIC (50865-710-17)Marketed from Oct 1, 2015 | |
| 50865-710-41 | 5086507104150865071041 | 1000 mL in 1 BAG (50865-710-41)Marketed from Dec 1, 2015 | |
| 50865-710-44 | 5086507104450865071044 | 1000 mL in 1 BAG (50865-710-44)Marketed from Oct 1, 2015 | |
| 50865-710-55 | 5086507105550865071055 | 1200 mL in 1 BAG (50865-710-55)Marketed from Oct 1, 2015 | |
| 50865-710-91 | 5086507109150865071091 | 532 mL in 1 BOTTLE, PUMP (50865-710-91)Marketed from Oct 1, 2015 | |
| 50865-710-92 | 5086507109250865071092 | 59 mL in 1 BOTTLE (50865-710-92)Marketed from Apr 24, 2026 |
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)
- alcohol
- Active ingredients
- Alcohol — .072 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 50865-710_50375794-9187-674e-e063-6394a90a6dffSPL ID 50375794-9187-674e-e063-6394a90a6dffSPL set ID b2e22e51-88f5-4391-8705-3855c1645d80UNII 3K9958V90M
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
N450865071017followed by a unit qualifier and the quantityPackage 50865-0710-17. 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 Hand sanitizer to help reduce bacteria on the skin that could cause disease.
Excerpt only. Read the full label for complete information.
About NDC 50865-710
- What is NDC 50865-710?
- 50865-710 is the product NDC for Foaming Sanitizing Hand (alcohol), Alcohol .072 mg/mL soap, listed with the FDA by Kutol Products Company. It has 6 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Foaming Sanitizing Hand (Alcohol).
- What is the active ingredient?
- Alcohol.
- 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 Handbenzalkonium chloride | Benzalkonium chloride .003 mg/mL | SoapTopical | Kutol Products Company | 50865-683 | 50865-0683-0450865-0683-1750865-0683-41+1 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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