About this document
Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 077789
· View the label on DailyMed
Revision date stated in the text: October 2018
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Drug information for Chlorhexidine
| Rx or OTC |
Prescription (Rx)?
- This drug is available only with a prescription from a licensed healthcare provider.
- Rx
|
| Active ingredient |
Chlorhexidine gluconate 1.2 mg/mL
|
| Dosage form |
Liquid |
| Route |
Buccal |
| Marketing status |
listed in the FDA NDC Directory |
| Company (applicant) |
PHARMOBEDIENT |
| FDA approval |
ANDA 077789Abbreviated New Drug Application (ANDA) – generic drug
Approved June 18, 2009
|
| Therapeutic equivalence (TE) code |
ATCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book). |
| Manufacturers |
12 labelers list this drug on DailyMed |
| Packages (NDC) |
| Package |
|
1.2 mg/mL – 15 ml in 1 bottle
NDC 53462-003-15
|
|
Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.