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DASH Chlorhexidine Gluconate 0.12% Oral Rinse 1.2 mg/mL oral liquid

Chlorhexidine · Oral · Natco Pharma
Available on requestPrescription onlyUS FDAIndian manufacturer

DASH Chlorhexidine Gluconate 0.12% Oral Rinse 1.2 mg/mL oral liquid is a prescription medicine containing Chlorhexidine for oral use, marketed by Natco Pharma, 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

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-86°F).

Key facts

Active ingredient (INN)
Chlorhexidine
Brand
DASH Chlorhexidine Gluconate 0.12% Oral Rinse
Strength
1.2 mg/mL
Dosage form
Oral liquid
Route
Oral
Packs
15 mL, 600 mL, 1500 mL and 2 more
Marketing authorisation holder
Natco Pharma
Manufacturers
Natco PharmaIndiaCardinal Health
Origin register
US FDA, United States
Storage
Store at 20°-25°C (68°-77°F), excursions permitted to 15°-30°C (59°-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
25 April 2018
Identifiers
RxCUI 834127DailyMed set ID 12a11cd7-5087-4eb8-aa52-4fad402450f7, 0253513c-148c-4be7-a6d5-5528f40806fa, acc9ac8e-6f1c-4fcb-880d-dcc03d411ed3NDC 69339-138, 55154-1980, 55154-1981Application ANDA074291

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

PackCodeLabelerMarketed since
15 mL in 1 cup, unit-dose69339-138-15Natco PharmaIndia25 April 2018
600 mL in 1 dose pack69339-138-17Natco PharmaIndia25 April 2018
1500 mL in 1 dose pack69339-138-19Natco PharmaIndia25 April 2018
5 cup, unit-dose in 1 bag / 15 mL in 1 cup, unit-dose55154-1980-5Cardinal Health25 April 2018
5 cup, unit-dose in 1 bag / 15 mL in 1 cup, unit-dose55154-1981-5Cardinal Health25 April 2018

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.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 17 September 1976Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS 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 liquid.

Compare all 3

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 Chlorhexidine

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need DASH Chlorhexidine Gluconate 0.12% Oral Rinse 1.2 mg/mL oral liquid 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.