Over-the-counter drug · OTC MONOGRAPH DRUG
Foaming Hand Sanitizer (Benzalkonium chloride) NDC 83986-118
Benzalkonium chloride 1.3 mg/mL · Liquid · Topical · UpLift Brands LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83986-118-45 | 8398601184583986011845 | 1150 mL in 1 BOTTLE, PLASTIC (83986-118-45)Marketed from Feb 29, 2024 | |
| 83986-118-86 | 8398601188683986011886 | 1000 mL in 1 BOTTLE, PLASTIC (83986-118-86)Marketed from Feb 29, 2024 | |
| 83986-118-96 | 8398601189683986011896 | 221 mL in 1 BOTTLE, PLASTIC (83986-118-96)Marketed from Feb 29, 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)
- Foaming Hand Sanitizer
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- UpLift Brands LLCNDC labeler code 83986
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 83986-118_5c26fadc-8cf0-669c-e063-6394a90aa52fSPL ID 5c26fadc-8cf0-669c-e063-6394a90aa52f
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
N483986011845followed by a unit qualifier and the quantityPackage 83986-0118-45. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 83986-118
- What is NDC 83986-118?
- 83986-118 is the product NDC for Foaming Hand Sanitizer (benzalkonium chloride), Benzalkonium chloride 1.3 mg/mL liquid, listed with the FDA by UpLift Brands LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Foaming Hand Sanitizer (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- UpLift Brands LLC, NDC labeler code 83986. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Foaming Hand Sanitizer?
- 2 other product NDCs are listed under this name. See all Foaming Hand Sanitizer NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Foaming Hand Sanitizer products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Foaming Hand Sanitizerhand sanitizer | Benzalkonium chloride 1.3 g/1000mL | LiquidTopical | American Chemical Systems II, LLC | 75044-280 | 75044-0280-1675044-0280-31 |
| Foaming Hand Sanitizeralcohol | Alcohol 70 mL/100mL | SolutionTopical | Empack Spraytech Inc. | 50021-020 | 50021-0020-0150021-0020-02 |
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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