Over-the-counter drug · OTC MONOGRAPH DRUG
Kay Foaming Antibacterial Handsoap (Chloroxyenol) NDC 47593-661
Chloroxylenol 5 mg/mL · Solution · Topical · Ecolab Inc.
NDC codes
FDA NDC DirectoryProduct information
- Brand name (proprietary)
- Kay Foaming Antibacterial Handsoap
- Generic name (nonproprietary)
- chloroxyenol
- Active ingredients
- Chloroxylenol — 5 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- Ecolab Inc.NDC labeler code 47593
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 47593-661_b7be6ed8-69ff-40a3-a7cf-d3359e110e36SPL ID b7be6ed8-69ff-40a3-a7cf-d3359e110e36SPL set ID f572be64-6af9-4b4b-bd5b-cd031608de24RxCUI 436367UNII 0F32U78V2Q
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.
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses For handwashing to decrease bacteria on the skin.
Excerpt only. Read the full label for complete information.
About NDC 47593-661
- What is NDC 47593-661?
- 47593-661 is the product NDC for Kay Foaming Antibacterial Handsoap, Chloroxylenol 5 mg/mL solution, listed with the FDA by Ecolab Inc..
- What drug is associated with this NDC?
- Kay Foaming Antibacterial Handsoap (Chloroxyenol).
- What is the active ingredient?
- Chloroxylenol.
- Who is the labeler?
- Ecolab Inc., NDC labeler code 47593. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Kay Foaming Antibacterial Handsoap?
- 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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