Over-the-counter drug · OTC MONOGRAPH DRUG
Antiseptic Foaming Hand Sanitizer (Benzalkonium chloride) NDC 82442-812
Benzalkonium chloride 1.3 mg/mL · Liquid · Topical · Target Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 82442-812-20 | 8244208122082442081220 | 2 BOTTLE, PLASTIC in 1 CARTON (82442-812-20) / 88 mL in 1 BOTTLE, PLASTICMarketed from Oct 11, 2024 |
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)
- Antiseptic Foaming Hand Sanitizer
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Target CorporationNDC labeler code 82442
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 82442-812_4b1f871e-4c37-6d61-e063-6294a90ae28eSPL ID 4b1f871e-4c37-6d61-e063-6294a90ae28eSPL set ID 93d6e4df-9428-4557-b251-c7aa9bda3412RxCUI 1020365UNII F5UM2KM3W7
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
N482442081220followed by a unit qualifier and the quantityPackage 82442-0812-20. 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)
Use to decrease bacteria on the skin
Excerpt only. Read the full label for complete information.
About NDC 82442-812
- What is NDC 82442-812?
- 82442-812 is the product NDC for Antiseptic Foaming Hand Sanitizer, Benzalkonium chloride 1.3 mg/mL liquid, listed with the FDA by Target Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Antiseptic Foaming Hand Sanitizer (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Target Corporation, NDC labeler code 82442. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Antiseptic 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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