Chlorhexidine Gluconate 0.12% Oral Rinse NDC 68999-650

NDC codes

FDA NDC Directory

Product NDC (as listed)68999-650Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68999-0650Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68999-650-24	68999065024	2 TRAY in 1 BOX (68999-650-24) / 10 CUP in 1 TRAY / 15 mL in 1 CUP (68999-650-51)Marketed from Jan 8, 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): Chlorhexidine Gluconate 0.12% Oral Rinse
Generic name (nonproprietary): chlorhexidine gluconate 0.12% oral rinse
Active ingredients: Chlorhexidine gluconate — 1.2 mg/mL
Dosage form: Solution
Route: Oral
Labeler: Chartwell Governmental & Specialty RX, LLC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075006
Marketing start: Mar 3, 2004
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Cell Wall Integrity (Physiologic effect)
Identifiers: Product ID 68999-650_47f94c38-483e-2001-e063-6394a90a9d05SPL ID 47f94c38-483e-2001-e063-6394a90a9d05SPL set ID 8c71f7a2-7c35-4897-b850-de677a34f5bdRxCUI 834127UNII MOR84MUD8E

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

N468999065024 followed by a unit qualifier and the quantity

Package 68999-0650-24. 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 Jan 9, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Chlorhexidine gluconate oral rinse 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. Chlorhexidine gluconate oral rinse 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.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075006

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 075006
Product	Strength	Form · route	Labeler	Product NDC
Chlorhexidine Gluconate 0.12% Oral Rinse	Chlorhexidine gluconate 1.2 mg/mL	SolutionOral	Chartwell RX, LLC	62135-649
Chlorhexidine Gluconate 0.12% Oral Rinse	Chlorhexidine gluconate 1.2 mg/mL	SolutionOral	Chartwell RX, LLC	62135-650