Medicine
Peridex 1.2 mg/mL oral rinse
Peridex 1.2 mg/mL oral rinse is a prescription medicine containing Chlorhexidine for oral use, marketed by Solventum, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
STORE at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C…
Key facts
- Active ingredient (INN)
- Chlorhexidine
- Brand
- Peridex
- Strength
- 1.2 mg/mL
- Dosage form
- Oral rinse
- Route
- Oral
- Packs
- 473 mL, 1893 mL, 118 mL
- Marketing authorisation holder
- Solventum
- Manufacturer
- Solventum
- Origin register
- US FDA, United States
- Storage
- STORE at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F).
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- A01AB03 Chlorhexidine
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 13 August 1986
- Identifiers
- RxCUI 834127, 834135DailyMed set ID 3fcd41c4-875a-4e54-b533-261f198011afNDC 48878-0620Application NDA019028
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 17 September 1976 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Alternatives
Other makers and brands of Chlorhexidine 1.2 mg/mL oral rinse.
- Chlorhexidine 1.2 mg/mL oral rinseAvailable on request—US FDA33 packs
- Periogard Alcohol Free 1.2 mg/mL oral rinseAvailable on requestColgate Oral PharmaceuticalsUS FDA5 packs
- NUPRO Chlorhexidine Gluconate 1.2 mg/mL oral rinseAvailable on requestDentsply LLC. Professional Division Trading as "DENTSPLY Professional"US FDA2 packs
- Sky Oral Rinse 1.2 mg/mL oral rinseAvailable on requestMcKessonUS FDA3 packs
- Chlorhexidine 1.2 mg/mL oral rinseAvailable on request—US FDA2 packs
- Chlorhexidine 1.2 mg/mL oral rinseAvailable on request—US FDA2 packs
Other strengths and forms of Chlorhexidine
Clinical summary
Chlorhexidine is a prescription medicine. It is available as oral rinse, solution and oral liquid for dental and buccal use. MedsAcross supplies Chlorhexidine for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about ChlorhexidineFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- ANTISEPTIC SKIN CLEANSER prescribing information (Xttrium Laboratories) · U.S. National Library of Medicine, DailyMed
Need Peridex 1.2 mg/mL oral rinse for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.