Overview
Aluminum chloride is a chemical compound with the chemical formula AlCl3. When contaminated with iron chloride, it often displays a yellow color compared to the white pure compound. It is used in various chemical applications as a Lewis base, with anhydrous aluminium trichloride being the most commonly used Lewis acid. It may also be found in over-the-counter as an antiperspirant or prescription products as an antihemorrhagic agent. In antiperspirant products, FDA approves the use of aluminum chloride as an active ingredient up to 15%, calculated on the hexahydrate form, in an aqueous solution nonaerosol dosage form .
Indication
No indication information available.
Associated Conditions
- Excessive sweating and body odor
- Hyperphosphataemia
- Minor bleeding
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 |
|---|---|---|---|---|---|
| Henry Schein | 0404-1080 | DENTAL | 250 mg in 1 g | 5/13/2010 | |
| Medical Products Laboratories, Inc. | 10733-412 | TOPICAL | 250 mg in 1 g | 12/23/2020 | |
| Cargus International, Inc. | 61509-100 | DENTAL | 7500 mg in 30 mL | 2/1/2019 | |
| Pearson Dental Supplies INC. | 43305-0000 | DENTAL | 7500 mg in 30 mL | 1/19/2022 | |
| IQ Dental Supply, LLC | 42756-1100 | DENTAL | 7500 mg in 30 mL | 1/27/2022 | |
| Benco Dental | 66975-359 | DENTAL | 7500 mg in 30 mL | 1/24/2022 | |
| Scott's Dental Supply LLC | 69638-059 | DENTAL, ORAL, TOPICAL | 7500 mg in 30 mL | 3/12/2020 | |
| Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc. | 68400-203 | DENTAL | 7500 mg in 30 mL | 1/20/2022 | |
| Dharma Research, inc. | 53045-300 | DENTAL, TOPICAL, ORAL | 8.75 g in 35 g | 11/6/2020 |
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 |
|---|---|---|---|---|---|
| Racestyptine Solution bottle | 23162 | Medicine | A | 10/14/1991 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| ALUMINIUM MURIATICUM GRANULE 3DH-30DH | homeocan inc. | 01933167 | Tablet - Oral | 3 DH | 12/31/1991 |
| GINGIGEL GEL 200MG/GM | van r dental products inc. | 00687588 | Gel - Topical | 200 MG / G | 12/31/1986 |
| GINGI AID DARK BRAID #1 | gingi-pak labs, division of belport co., inc. | 00539341 | Cord - Dental
,
Topical | 1 MG / 2.54 CM | 12/31/1981 |
| GINGI AID DARK BRAID #3 | gingi-pak labs, division of belport co., inc. | 00479381 | Cord - Dental | 1 MG / 2.54 CM | 12/31/1981 |
| GINGI AID DARK BRAID #2 | gingi-pak labs, division of belport co., inc. | 00539341 | Cord - Dental
,
Topical | 1 MG / 2.54 CM | 12/31/1981 |
| GINGI AID 10% | gingi-pak labs, division of belport co., inc. | 00479357 | Liquid - Dental | 100 MG / ML | 12/31/1979 |
| AQUASTOP LIQ | aqua laboratories | 00399868 | Liquid - Topical | 20 % | 12/31/1977 |
| LEXXEL IDS | vivier canada incorporated | 02237838 | Gel - Topical | 23 % | N/A |
| YOUTH DEW ROLL ON ANTIPERSP DEOD LOT | estee lauder dist. | 00629065 | Lotion - Topical | 2 % | 12/31/1986 |
| RACESTYPTINE SOL | 00379638 | Liquid - Dental | 25 G / 100 ML | 12/31/1977 |
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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