Overview
Potassium carbonate (K2CO3) is a white salt, soluble in water (insoluble in ethanol) which forms a strongly alkaline solution. It can be made as the product of potassium hydroxide's absorbent reaction with carbon dioxide. It presents a large capacity to absorb moisture.
Indication
Not Available
Associated Conditions
- Fungal skin infection
- Parasitic skin infections
- Psoriasis
- Seborrheic Dermatitis
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 |
---|---|---|---|---|---|
Deseret Biologicals, Inc. | 43742-2108 | ORAL | 8 [hp_X] in 1 mL | 5/27/2025 | |
King Bio Inc. | 57955-2822 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
Deseret Biologicals, Inc. | 43742-2265 | ORAL | 30 [hp_C] in 1 mL | 5/6/2025 | |
Deseret Biologicals, Inc. | 43742-1573 | ORAL | 30 [hp_C] in 1 mL | 5/27/2025 | |
King Bio Inc. | 57955-2828 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
Deseret Biologicals, Inc. | 43742-1312 | ORAL | 8 [hp_X] in 1 mL | 5/27/2025 | |
Dr. Donna Restivo DC | 62185-0062 | ORAL | 8 [hp_X] in 1 mL | 5/23/2025 | |
Newton Laboratories, Inc. | 55714-1736 | ORAL | 15 [hp_X] in 1 g | 5/7/2025 | |
Apotheca Company | 57520-0228 | ORAL | 200 [hp_X] in 1 mL | 6/9/2025 | |
Newton Laboratories, Inc. | 55714-1536 | ORAL | 15 [hp_X] in 1 mL | 5/7/2025 |
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 |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
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 |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Concord StemCL Plus | 398617 | Medicine | A | 10/31/2022 | |
CHLORVESCENT potassium 14 mmol effervescent tablet tube (reformulation) | 71981 | Medicine | A | 12/1/1999 | |
BIOLOGICAL THERAPIES C-SALTS EFFERVESCENT | 22420 | Medicine | A | 10/8/1991 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
R-24 DPS | dr reckeweg canada | 02090449 | Drops - Oral | 6 D / 10 ML | 12/31/1994 |
POUR IT ON THICK | kootenay born botanicals | 02232067 | Syrup - Oral | 12 X | 5/25/1998 |
POTASSIUM CARBONATE LIQUID (S#140) | total health centre | 02197073 | Liquid - Sublingual | 2 X / ML | 6/1/1997 |
HOMEOPATHIC MEDICINE (S140) DPS 30C | total health centre | 02071495 | Drops - Oral | 30 C / ML | 12/31/1994 |
CORA-BOSAN B43 - TAB | professional health products | 02157713 | Tablet - Oral | 2 D | 12/31/1996 |
KALIUM CARB GOUTTE 1DH-30CH | boiron laboratoires | 00671290 | Drops - Oral | 1 DH / DH | 12/31/1987 |
KALIUM CARBONICUM | seroyal international inc. | 02233157 | Globules
,
Liquid
,
Drops
,
Pellet
,
Granules
,
Tablet - Oral | 2 X | 4/6/1998 |
TUSNIX SYRUP | terra botanica products ltd. | 02233376 | Liquid - Oral | 12 X | 2/2/1998 |
ANAGALLIS COMP. PELLETS | 02232696 | Pellet - Oral | 5 D | 4/10/1998 | |
ASTH HP | bio active canada ltd. | 02233555 | Liquid - Oral | 30 X | 5/26/1998 |
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. |
Help Us Improve
Your feedback helps us provide better drug information and insights.