Over-the-counter drug · OTC MONOGRAPH DRUG
Benzalkonium chloride NDC 79903-459
Benzalkonium chloride 1.3 mg/mL · Liquid · Topical · WALMART INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 79903-459-11 | 7990304591179903045911 | 332 mL in 1 BOTTLE (79903-459-11)Marketed from Oct 12, 2026 |
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)
- Benzalkonium chloride
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1.3 mg/mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- WALMART INC.NDC labeler code 79903
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 79903-459_a401aca3-1542-4b11-b4b2-70bbba8e4b7dSPL ID a401aca3-1542-4b11-b4b2-70bbba8e4b7d
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
N479903045911followed by a unit qualifier and the quantityPackage 79903-0459-11. 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 79903-459
- What is NDC 79903-459?
- 79903-459 is the product NDC for Benzalkonium chloride, Benzalkonium chloride 1.3 mg/mL liquid, listed with the FDA by WALMART INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Benzalkonium chloride.
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- WALMART INC., NDC labeler code 79903. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Benzalkonium chloride?
- 32 other product NDCs are listed under this name. See all Benzalkonium chloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Benzalkonium chloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Benzalkonium chloride | Benzalkonium chloride .13 mg/mL | SwabTopical | UpLift Brands, LLC | 83986-912 | 83986-0912-2083986-0912-90 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-094 | 59640-0094-4559640-0094-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-149 | 59640-0149-4559640-0149-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-252 | 59640-0252-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-273 | 59640-0273-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-290 | 59640-0290-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-306 | 59640-0306-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-317 | 59640-0317-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-321 | 59640-0321-96 |
| Benzalkonium Chloride | Benzalkonium chloride 1.3 mg/mL | LiquidTopical | H E B | 59640-373 | 59640-0373-96 |
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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