Over-the-counter drug · OTC MONOGRAPH DRUG
Refresh AntiBac FOAM (Benzalkonium chloride) NDC 11084-010
Benzalkonium chloride .13 g/L · Soap · Topical · SC Johnson Professional USA Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 11084-010-05 | 1108400100511084001005 | 3.78 L in 1 BOTTLE, PLASTIC (11084-010-05)Marketed from Jun 12, 2017 | |
| 11084-010-12 | 1108400101211084001012 | 1.2 L in 1 BOTTLE, PLASTIC (11084-010-12)Marketed from Jun 12, 2017 | |
| 11084-010-20 | 1108400102011084001020 | 2 L in 1 BOTTLE, PLASTIC (11084-010-20)Marketed from Jun 12, 2017 | |
| 11084-010-66 | 1108400106611084001066 | 1 L in 1 BOTTLE, PLASTIC (11084-010-66)Marketed from Dec 31, 2022 |
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)
- Refresh AntiBac FOAM
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — .13 g/L
- Dosage form
- Soap
- Route
- Topical
- Labeler
- SC Johnson Professional USA Inc.NDC labeler code 11084
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 11084-010_1efa3243-2522-4796-9891-a61fc315ea00SPL ID 1efa3243-2522-4796-9891-a61fc315ea00SPL set ID 884d1c8c-5643-423e-8ed4-d2ef38f8af73RxCUI 1046593UNII F5UM2KM3W7UPC 0069124050070
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
N411084001005followed by a unit qualifier and the quantityPackage 11084-0010-05. 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 reduce bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 11084-010
- What is NDC 11084-010?
- 11084-010 is the product NDC for Refresh AntiBac FOAM (benzalkonium chloride), Benzalkonium chloride .13 g/L soap, listed with the FDA by SC Johnson Professional USA Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Refresh AntiBac FOAM (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- SC Johnson Professional USA Inc., NDC labeler code 11084. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Refresh AntiBac 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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