Over-the-counter drug · OTC MONOGRAPH DRUG
eZFoam Foaming Alcohol Hand Sanitizer (Foaming hand sanitizer) NDC 50865-688
Alcohol 62 mL/100mL · Solution · Topical · Kutol Products Company
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50865-688-09 | 5086506880950865068809 | 3785 mL in 1 JUG (50865-688-09)Marketed from Jun 27, 2013 | |
| 50865-688-17 | 5086506881750865068817 | 50 mL in 1 BOTTLE, PLASTIC (50865-688-17)Marketed from Jun 27, 2013 | |
| 50865-688-24 | 5086506882450865068824 | 1000 mL in 1 BAG (50865-688-24)Marketed from Jun 27, 2013 | |
| 50865-688-41 | 5086506884150865068841 | 1000 mL in 1 BAG (50865-688-41)Marketed from Jun 27, 2013 | |
| 50865-688-50 | 5086506885050865068850 | 1200 mL in 1 BAG (50865-688-50)Marketed from Jun 27, 2013 | |
| 50865-688-78 | 5086506887850865068878 | 950 mL in 1 BOTTLE, PLASTIC (50865-688-78)Marketed from Jun 27, 2013 |
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)
- eZFoam Foaming Alcohol Hand Sanitizer
- Generic name (nonproprietary)
- foaming hand sanitizer
- Active ingredients
- Alcohol — 62 mL/100mL
- Dosage form
- Solution
- 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 50865-688_298e167d-7005-98da-e063-6294a90a07baSPL ID 298e167d-7005-98da-e063-6294a90a07baSPL set ID 1f56b4c5-d703-4193-83a8-3be815c8acdaRxCUI 616763UNII 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
N450865068809followed by a unit qualifier and the quantityPackage 50865-0688-09. 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)
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use. Avoid contact with eyes. If eye contact occurs, flush with water. Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, contact a physician or poison control center.
Excerpt only. Read the full label for complete information.
About NDC 50865-688
- What is NDC 50865-688?
- 50865-688 is the product NDC for eZFoam Foaming Alcohol Hand Sanitizer, Alcohol 62 mL/100mL solution, 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?
- eZFoam Foaming Alcohol Hand Sanitizer (Foaming Hand Sanitizer).
- 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 eZFoam Foaming Alcohol 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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