Over-the-counter drug · OTC MONOGRAPH DRUG
Alcohol-Free Hand Sanitizing Foam (Benzalkonium chloride) NDC 63998-764
Benzalkonium chloride 1 mg/mL · Solution · Topical · United Laboratories Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63998-764-01 | 6399807640163998076401 | 59 mL in 1 BOTTLE (63998-764-01)Marketed from Jan 1, 2019 | |
| 63998-764-02 | 6399807640263998076402 | 750 mL in 1 BOTTLE (63998-764-02)Marketed from Jan 1, 2019 |
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 Hand Sanitizing Foam
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- United Laboratories Inc.NDC labeler code 63998
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 63998-764_27c4d6fe-7567-073f-e063-6394a90afe9fSPL ID 27c4d6fe-7567-073f-e063-6394a90afe9fSPL set ID 4f5ddead-1868-45c2-9657-762c9ca3a0e2RxCUI 1038799UNII 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
N463998076401followed by a unit qualifier and the quantityPackage 63998-0764-01. 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 hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.
Excerpt only. Read the full label for complete information.
About NDC 63998-764
- What is NDC 63998-764?
- 63998-764 is the product NDC for Alcohol-Free Hand Sanitizing Foam, Benzalkonium chloride 1 mg/mL solution, listed with the FDA by United Laboratories Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Alcohol-Free Hand Sanitizing Foam (Benzalkonium chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- United Laboratories Inc., NDC labeler code 63998. 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 Hand Sanitizing Foam?
- 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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