Over-the-counter drug · OTC MONOGRAPH DRUG
Alcohol Free Foaming Hand Sanitizer (Benzalkonium chloride) NDC 65601-700
Benzalkonium chloride 1.3 mg/mL · Soap · Topical · Betco Corporation, Ltd.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 65601-700-04 | 6560107000465601070004 | 3780 mL in 1 BOTTLE, PLASTIC (65601-700-04)Marketed from Jan 1, 2016 | |
| 65601-700-29 | 6560107002965601070029 | 1000 mL in 1 BAG (65601-700-29)Marketed from Jan 1, 2016 | |
| 65601-700-53 | 6560107005365601070053 | 50 mL in 1 BOTTLE, PUMP (65601-700-53)Marketed from Jan 1, 2016 | |
| 65601-700-55 | 6560107005565601070055 | 207900 mL in 1 DRUM (65601-700-55)Marketed from Jan 1, 2016 | |
| 65601-700-88 | 6560107008865601070088 | 500 mL in 1 BOTTLE, PUMP (65601-700-88)Marketed from Nov 12, 2012 |
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)
- Alcohol Free Foaming Hand Sanitizer
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Soap
- Route
- Topical
- Labeler
- Betco Corporation, Ltd.NDC labeler code 65601
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 65601-700_5b10cc05-8b62-deb8-e063-6394a90a9b8cSPL ID 5b10cc05-8b62-deb8-e063-6394a90a9b8cSPL set ID 7e038b0a-4813-4f4b-ad66-0584d75a064fRxCUI 1020365UNII F5UM2KM3W7UPC 0700427023810, 0700427006516, 0700427015303, 0700427031761, 0700427028204
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
N465601070004followed by a unit qualifier and the quantityPackage 65601-0700-04. 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)
Alcohol Free Foaming Hand Sanitizer Uses Hand sanitizer to remove microorganisms on the skin. Use this product when soap and water are not available.
Excerpt only. Read the full label for complete information.
About NDC 65601-700
- What is NDC 65601-700?
- 65601-700 is the product NDC for Alcohol Free Foaming Hand Sanitizer, Benzalkonium chloride 1.3 mg/mL soap, listed with the FDA by Betco Corporation, Ltd.. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Alcohol Free Foaming Hand Sanitizer (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Betco Corporation, Ltd., NDC labeler code 65601. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Alcohol Free Foaming Hand Sanitizer?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
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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