Overview
Sodium Carbonate is the disodium salt of carbonic acid with alkalinizing property. When dissolved in water, sodium carbonate forms carbonic acid and sodium hydroxide. As a strong base, sodium hydroxide neutralizes gastric acid thereby acting as an antacid.
Indication
Used topically for dermatitides, mouthwash, vaginal douche; veterinary use as emergency emetic.Occasionally, for dermatitides topically as a lotion. Medication (Vet): In solution to cleanse skin, in eczema, to soften scabs of ringworm.
Associated Conditions
- Impacted ear wax
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Newton Laboratories, Inc. | 55714-2465 | ORAL | 15 [hp_X] in 1 mL | 8/20/2025 | |
| King Bio Inc. | 57955-9150 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 | |
| Newton Laboratories, Inc. | 55714-2466 | ORAL | 15 [hp_X] in 1 g | 8/20/2025 | |
| Direct Outlet Supplier LLC | 85813-001 | RESPIRATORY (INHALATION) | 10 g in 100 g | 9/3/2025 | |
| Deseret Biologicals, Inc. | 43742-2185 | ORAL | 6 [hp_X] in 1 mL | 5/27/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| CEFAZIME FOR INJECTION 1 g/vial | SIN11470P | INJECTION | 121 mg/vial | 3/26/2001 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| LEMON FLAVOURED ENO FRUIT SALT | N/A | N/A | N/A | 8/8/1983 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| ENO Lemon flavour powder | 40656 | Medicine | A | 7/30/1992 | |
| ENO REGULAR oral powder jar | 40655 | Medicine | A | 7/30/1992 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| HOMEO-FORM AR-TAB | homeocan inc. | 02149281 | Tablet - Oral | 4 X | 12/31/1995 |
| R48 DPS | dr reckeweg and co | 00857173 | Drops - Oral | 6 DH / DH | 12/31/1989 |
| ADAPTAGEN | bio active canada ltd. | 02233546 | Liquid - Oral | 12 X | 5/26/1998 |
| CARBICARB INJECTION | International Medication Systems Ltd. | 00757004 | Liquid - Intravenous | 35 MG / ML | 12/31/1992 |
| NATRIUM CARBONICUM-INJEEL FORTE N (6D,8D,12D,30D,200D/1.1ML) | 02051451 | Liquid - Oral | 6 D / 1.1 ML | 12/31/1993 | |
| HOMEO-FORM AL-TAB | homeocan inc. | 02149303 | Tablet - Oral | 6 X | 12/31/1995 |
| HEEL 166 TABLETS | 01969226 | Tablet - Oral | 3 DH / TAB | 12/31/1992 | |
| UROLOGIC SOLUTION G | baxter corporation | 00800015 | Liquid - Irrigation | 430 MG / 100 ML | 12/31/1989 |
| NATRUM CARBONICUM DPS C6-C1000 | thompson's homeopathic supplies ltd. | 00828270 | Drops - Oral | 6 C / C | 12/31/1989 |
| UROLOGIC G FOR IRRIGATION | ICU Medical Canada Inc | 00039365 | Solution - Irrigation | 2.2 MG / ML | 12/31/1969 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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