Over-the-counter drug · OTC MONOGRAPH DRUG
UP and UP (Benzalkonium chloride) NDC 82442-088
Benzalkonium chloride 130 mg/100mL · Liquid · Topical · TARGET CORPORATION INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 82442-088-07 | 8244200880782442008807 | 222 mL in 1 BOTTLE, PLASTIC (82442-088-07)Marketed from Oct 22, 2025 |
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)
- UP and UP
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 130 mg/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- TARGET CORPORATION INC.NDC labeler code 82442
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 82442-088_51531f24-f43f-f7d9-e063-6294a90a0394SPL ID 51531f24-f43f-f7d9-e063-6294a90a0394SPL set ID 39855595-cd79-a116-e063-6294a90a9638RxCUI 1046593UNII F5UM2KM3W7UPC 0191907923223
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
N482442008807followed by a unit qualifier and the quantityPackage 82442-0088-07. 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 hand washing to decrease bacteria on the skin.
Excerpt only. Read the full label for complete information.
About NDC 82442-088
- What is NDC 82442-088?
- 82442-088 is the product NDC for UP and UP (benzalkonium chloride), Benzalkonium chloride 130 mg/100mL liquid, listed with the FDA by TARGET CORPORATION INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- UP and UP (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- TARGET CORPORATION INC., 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 UP and UP?
- 1 other product NDC are listed under this name. See all UP and UP NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other UP and UP products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| up and upphenylephrine hydrochloride | Phenylephrine hydrochloride 6.25 mg/1 | SuppositoryRectal | Target Corporation | 82442-060 | 82442-0060-12 |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
Showing 20 of 40.