Over-the-counter drug · OTC MONOGRAPH DRUG
Dial Professional Antibacterial Foaming Hand Wash Spring Water NDC 54340-140
dial professional antibacterial foaming hand soap spring water scent · Benzalkonium chloride .13 g/100mL · Liquid · Topical · Henkel Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 54340-140-02 | 5434001400254340014002 | 3 BOTTLE, DISPENSING in 1 CARTON (54340-140-02) / 1700 mL in 1 BOTTLE, DISPENSING (54340-140-01)Marketed from Jan 1, 2024 | |
| 54340-140-04 | 5434001400454340014004 | 3 BOTTLE, DISPENSING in 1 CARTON (54340-140-04) / 1200 mL in 1 BOTTLE, DISPENSING (54340-140-03)Marketed from Jan 1, 2024 | |
| 54340-140-06 | 5434001400654340014006 | 3 BOTTLE, DISPENSING in 1 CARTON (54340-140-06) / 1000 mL in 1 BOTTLE, DISPENSING (54340-140-05)Marketed from Jan 1, 2024 | |
| 54340-140-08 | 5434001400854340014008 | 3 BOTTLE, DISPENSING in 1 CARTON (54340-140-08) / 1200 mL in 1 BOTTLE, DISPENSING (54340-140-07)Marketed from Jan 1, 2024 | |
| 54340-140-09 | 5434001400954340014009 | 4 BOTTLE, DISPENSING in 1 CARTON (54340-140-09) / 3785 mL in 1 BOTTLE, DISPENSINGMarketed from Jan 1, 2024 | |
| 54340-140-10 | 5434001401054340014010 | 3 BOTTLE, DISPENSING in 1 CARTON (54340-140-10) / 1000 mL in 1 BOTTLE, DISPENSINGMarketed from Jan 1, 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)
- Dial Professional Antibacterial Foaming Hand Wash Spring Water
- Generic name (nonproprietary)
- dial professional antibacterial foaming hand soap spring water scent
- Active ingredients
- Benzalkonium chloride — .13 g/100mL
- Dosage form
- Liquid
- Route
- Topical
- Labeler
- Henkel CorporationNDC labeler code 54340
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 54340-140_458958bb-d833-0df7-e063-6394a90a3b04SPL ID 458958bb-d833-0df7-e063-6394a90a3b04SPL set ID 28dc867c-ca9b-4631-e063-6394a90a9a35RxCUI 1046593UNII F5UM2KM3W7UPC 0017000196923, 0023400828395
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
N454340014002followed by a unit qualifier and the quantityPackage 54340-0140-02. 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 54340-140
- What is NDC 54340-140?
- 54340-140 is the product NDC for Dial Professional Antibacterial Foaming Hand Wash Spring Water, Benzalkonium chloride .13 g/100mL liquid, listed with the FDA by Henkel Corporation. It has 6 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Dial Professional Antibacterial Foaming Hand Wash Spring Water (Dial Professional Antibacterial Foaming Hand Soap Spring Water Scent).
- What is the active ingredient?
- Benzalkonium chloride.
- Who is the labeler?
- Henkel Corporation, NDC labeler code 54340. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Dial Professional Antibacterial Foaming Hand Wash Spring Water?
- 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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