Over-the-counter drug · OTC MONOGRAPH DRUG
WhiskCare 377 (Benzalkonium chloride) NDC 65585-356
Benzalkonium chloride 1 mg/mL · Solution · Topical · Whisk Products, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 65585-356-01 | 6558503560165585035601 | 50 mL in 1 BOTTLE, PUMP (65585-356-01)Marketed from Feb 22, 2024 · Sample package | |
| 65585-356-02 | 6558503560265585035602 | 24 BOTTLE, PUMP in 1 BOTTLE (65585-356-02) / 50 mL in 1 BOTTLE, PUMPMarketed from Feb 22, 2024 | |
| 65585-356-03 | 6558503560365585035603 | 208198 mL in 1 DRUM (65585-356-03)Marketed from Feb 22, 2024 | |
| 65585-356-04 | 6558503560465585035604 | 4 BAG in 1 BOX (65585-356-04) / 1000 mL in 1 BAGMarketed from Feb 22, 2024 | |
| 65585-356-05 | 6558503560565585035605 | 8 BAG in 1 BOX (65585-356-05) / 1000 mL in 1 BAGMarketed from Feb 22, 2024 | |
| 65585-356-06 | 6558503560665585035606 | 6 BOTTLE, PUMP in 1 BOX (65585-356-06) / 550 mL in 1 BOTTLE, PUMPMarketed from Feb 22, 2024 | |
| 65585-356-08 | 6558503560865585035608 | 3785 mL in 1 BOTTLE, PLASTIC (65585-356-08)Marketed from Feb 22, 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)
- WhiskCare 377
- Generic name (nonproprietary)
- benzalkonium chloride
- Active ingredients
- Benzalkonium chloride — 1 mg/mL
- Dosage form
- Solution
- Route
- Topical
- Labeler
- Whisk Products, Inc.NDC labeler code 65585
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Marketing end
- Identifiers
- Product ID 65585-356_2206420a-400e-3a5f-e063-6394a90a49fdSPL ID 2206420a-400e-3a5f-e063-6394a90a49fdSPL set ID 124b403f-d12e-6e5c-e063-6394a90a63f8RxCUI 1038799UNII 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
N465585035601followed by a unit qualifier and the quantityPackage 65585-0356-01. 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 sanitizing to decrease bacteria on the skin Recommended for repeated use
Excerpt only. Read the full label for complete information.
About NDC 65585-356
- What is NDC 65585-356?
- 65585-356 is the product NDC for WhiskCare 377 (benzalkonium chloride), Benzalkonium chloride 1 mg/mL solution, listed with the FDA by Whisk Products, Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- WhiskCare 377 (Benzalkonium Chloride).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Whisk Products, Inc., NDC labeler code 65585. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for WhiskCare 377?
- 1 other product NDC are listed under this name. See all WhiskCare 377 NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other WhiskCare 377 products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| WhiskCare 377benzalkonium chloride | Benzalkonium chloride 1 mg/mL | SolutionTopical | Whisk Products, Inc. | 65585-529 | 65585-0529-0165585-0529-0265585-0529-03+4 more |
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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