Over-the-counter drug · OTC MONOGRAPH DRUG
ProCure Foaming Hand Sanitizer (Ethyl alcohol 72%) NDC 55681-040
Alcohol 72 mL/100mL · Gel · Topical · Twin Med LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55681-040-10 | 5568100401055681004010 | 1000 mL in 1 CARTRIDGE (55681-040-10)Marketed from Sep 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)
- ProCure Foaming Hand Sanitizer
- Generic name (nonproprietary)
- ethyl alcohol 72%
- Active ingredients
- Alcohol — 72 mL/100mL
- Dosage form
- Gel
- Route
- Topical
- Labeler
- Twin Med LLCNDC labeler code 55681
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 55681-040_52f7e8b4-f263-b053-e063-6394a90ae47aSPL ID 52f7e8b4-f263-b053-e063-6394a90ae47aSPL set ID 3d848ec8-5197-6d39-e063-6394a90aaef6RxCUI 2277550UNII 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
N455681004010followed by a unit qualifier and the quantityPackage 55681-0040-10. 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 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 55681-040
- What is NDC 55681-040?
- 55681-040 is the product NDC for ProCure Foaming Hand Sanitizer (ethyl alcohol 72%), Alcohol 72 mL/100mL gel, listed with the FDA by Twin Med LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- ProCure Foaming Hand Sanitizer (Ethyl Alcohol 72%).
- What is the active ingredient?
- Alcohol.
- Who is the labeler?
- Twin Med LLC, NDC labeler code 55681. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for ProCure 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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