Over-the-counter drug · OTC MONOGRAPH DRUG
North Woods Derma Foam E-2 (Benzalkonium chloride) NDC 53125-817
Benzalkonium chloride 1.3 mg/mL · Soap · Topical · Superior Chemical Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 53125-817-29 | 5312508172953125081729 | 1000 mL in 1 BAG (53125-817-29)Marketed from Sep 15, 2016 |
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)
- North Woods Derma Foam E-2
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Soap
- Route
- Topical
- Labeler
- Superior Chemical CorporationNDC labeler code 53125
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 53125-817_2736622c-4ecb-472d-e063-6394a90aa9dbSPL ID 2736622c-4ecb-472d-e063-6394a90aa9dbSPL set ID ab982dec-639a-277a-e053-2a95a90ac8b4RxCUI 1046593UNII F5UM2KM3W7UPC 0814410022411
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
N453125081729followed by a unit qualifier and the quantityPackage 53125-0817-29. 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 handwashing to decrease the bacteria on the skin. Recommended for repeated use.
Excerpt only. Read the full label for complete information.
About NDC 53125-817
- What is NDC 53125-817?
- 53125-817 is the product NDC for North Woods Derma Foam E-2 (benzalkonium chloride), Benzalkonium chloride 1.3 mg/mL soap, listed with the FDA by Superior Chemical Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- North Woods Derma Foam E-2 (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Superior Chemical Corporation, NDC labeler code 53125. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for North Woods Derma Foam E-2?
- 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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