Prescription drug · NDA
Peridex (Chlorhexidine gluconate) NDC 48878-0620
Chlorhexidine gluconate 1.2 mg/mL · Rinse · Oral · Solventum US LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 48878-0620-1 | 48878062001 | 473 mL in 1 BOTTLE (48878-0620-1)Marketed from Aug 13, 1986 | |
| 48878-0620-2 | 48878062002 | 1893 mL in 1 BOTTLE, DISPENSING (48878-0620-2)Marketed from Jan 16, 2013 | |
| 48878-0620-3 | 48878062003 | 118 mL in 1 BOTTLE (48878-0620-3)Marketed from Jan 16, 2013 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Peridex
- Generic name (nonproprietary)
- chlorhexidine gluconate
- Active ingredients
- Chlorhexidine gluconate — 1.2 mg/mL
- Dosage form
- Rinse
- Route
- Oral
- Labeler
- Solventum US LLCNDC labeler code 48878
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 019028
- Marketing start
- Listing expires
- Other FDA classes
- Decreased Cell Wall Integrity (Physiologic effect)
- Identifiers
- Product ID 48878-0620_88264ba1-fa70-4e87-8289-a48539ce55aaSPL ID 88264ba1-fa70-4e87-8289-a48539ce55aaSPL set ID 3fcd41c4-875a-4e54-b533-261f198011afRxCUI 834127, 834135UNII MOR84MUD8EUPC 0348878062011
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N448878062001followed by a unit qualifier and the quantityPackage 48878-0620-01. 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)
INDICATION: Peridex is indicated for use between dental visits as part of a professional program for the treatment of gingivitis as characterized by redness and swelling of the gingivae, including gingival bleeding upon probing. Peridex has not been tested among patients with acute necrotizing ulcerative gingivitis (ANUG). For patients having coexisting gingivitis and periodontitis, see PRECAUTIONS .
Excerpt only. Read the full label for complete information.
About NDC 48878-0620
- What is NDC 48878-0620?
- 48878-0620 is the product NDC for Peridex (chlorhexidine gluconate), Chlorhexidine gluconate 1.2 mg/mL rinse, listed with the FDA by Solventum US LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Peridex (Chlorhexidine gluconate).
- What is the active ingredient?
- Chlorhexidine gluconate.
- Who is the labeler?
- Solventum US LLC, NDC labeler code 48878. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Peridex?
- 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.