Overview
Phosphoric Acid is a colorless, odorless phosphorus-containing inorganic acid. Phosphoric acid is a sequestering agent which binds many divalent cations, including Fe++, Cu++, Ca++, and Mg++.
Indication
Phosphoric acid is used in dentistry and orthodontics as an etching solution, to clean and roughen the surfaces of teeth where dental appliances or fillings will be placed.
Associated Conditions
No associated conditions information available.
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 |
|---|---|---|---|---|---|
| The Wellness Center | 50181-0030 | ORAL | 1 [hp_M] in 1 mL | 5/28/2025 | |
| Dr. Masood Homeopathic Pharmaceuticals Private Limited | 82797-132 | ORAL | 0.01 mg in 120 mL | 4/24/2025 | |
| King Bio Inc. | 57955-9001 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 | |
| King Bio Inc. | 57955-5122 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 | |
| BioActive Nutritional, Inc. | 43857-0642 | ORAL | 12 [hp_X] in 1 mL | 5/20/2025 | |
| BioActive Nutritional, Inc. | 43857-0057 | ORAL | 12 [hp_X] in 1 mL | 5/20/2025 | |
| King Bio Inc. | 57955-1814 | ORAL | 12 [hp_X] in 236 mL | 5/20/2025 | |
| WellSpring Pharmaceutical Corporation | 65197-201 | ORAL | 21.5 mg in 5 mL | 6/10/2025 | |
| King Bio Inc. | 57955-9150 | ORAL | 10 [hp_X] in 59 mL | 5/19/2025 | |
| Bestmade Natural Products | 82969-5081 | ORAL | 30 [hp_C] in 30 [hp_C] | 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 |
|---|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|
| BRAUER CALM Oral Spray | 65600 | Medicine | A | 7/31/1998 | |
| FLUOROCARE 200 DAILY FLUORIDE MOUTH RINSE COOL MINT bottle | 78339 | Medicine | A | 5/3/2001 | |
| Hair Assist Women's Foam | 400972 | Medicine | A | 12/12/2022 | |
| Calm Oral Liquid | 492207 | Medicine | A | 6/19/2025 | |
| Calm Oral Liquid | 455427 | Medicine | A | 7/16/2024 | |
| Calm Oral Liquid | 345751 | Medicine | A | 10/12/2020 | |
| BRAUER CALM TABLETS | 65601 | Medicine | A | 7/31/1998 | |
| Cerebrum compositum | 93564 | Medicine | A | 3/20/2003 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| HOMEOPATHIC MEDICINE (S57) DPS 30C | total health centre | 02073420 | Drops - Oral | 30 C / ML | 12/31/1994 |
| ADAPTAGEN | bio active canada ltd. | 02233546 | Liquid - Oral | 12 X | 5/26/1998 |
| DIATHESIS IV | bio active canada ltd. | 02233601 | Liquid - Oral | 12 X | 5/26/1998 |
| HEMAREXIN LIQ | lab bio chimique inc.,division of technilab pharma inc. | 01922742 | Liquid - Oral | 13.75 MG / 5 ML | 12/22/1993 |
| ZIROXIDE MEDIUM FINE PASTE 1.23% FLUORIDE | medical products laboratories inc. | 02046881 | Paste - Nil
,
Dental | 0.4 % | 12/31/1994 |
| DENTI-CARE ACIDULATED PHOSPHATE FLUORIDE | 02239823 | Liquid - Dental | 52.5 G / 4.54 L | 11/26/1999 | |
| CUTISITUM | 02236489 | Liquid - Oral | 6 D | 2/6/1998 | |
| ACIDUM PHOSPHORICUM PLEX | seroyal international inc. | 02233076 | Pellet
,
Tablet
,
Drops
,
Syrup
,
Granules
,
Liquid - Oral | 3 X | 4/6/1998 |
| THC COMPLEX #59 | total health centre | 02236378 | Drops - Oral | 3 X | 3/29/1998 |
| PHOSPHORIC ACID PWR 6X | koegler laboratories inc. | 00858196 | Powder - Oral | 6 X / X | 12/31/1989 |
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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