Overview
Aluminum chlorohydrate is a group of water-soluble aluminum complexes with the general formula AlnCl(3n-m)(OH)m. It is included up to 25% in over-the-counter hygiene products as an active antiperspirant agent. The primary site of action of aluminum chlorohydrate is at the level of the stratum corneum layer, which is relatively near the skin surface . It is also used as a coagulant in the water purification process.
Indication
Indicated for use as an antiperspirant.
Associated Conditions
- Bullae of the feet
- Excessive sweating and body odor
- Hyperhidrosis
- Secondary infection Skin infection
- Sweating
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 |
|---|---|---|---|---|---|
| Rejoice International Corp. | 57337-173 | TOPICAL | 19 g in 100 g | 5/28/2025 | |
| Stock Your Home | 85505-395 | TOPICAL | 15 g in 100 1 | 4/22/2025 | |
| Rejoice International Corp. | 57337-172 | TOPICAL | 19 g in 100 g | 5/28/2025 | |
| Liufangjing Biotechnology (Yangzhou) Co., Ltd | 85420-001 | TOPICAL | 0.13 g in 1 g | 5/20/2025 |
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 |
|---|---|---|---|---|---|
| The Chemist Nappy Rash Paste | 14703 | Medicine | A | 10/25/1991 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| ARRID EXT DRY UNSCENT SPRAY AER 10% | carter products, division of carter wallace ns inc. | 00843105 | Aerosol - Topical | 10 % | 12/31/1989 |
| AVON ROLL ON ANTIPERSPIRANT DEODORANT VANILLA SOFT MUSK | the avon company canada limited | 02231128 | Lotion - Topical | 17.5 % | 3/13/1998 |
| AVON ROLL-ON ANTIPERSPIRANT DEODORANT FEELIN' FRESH POWDER BREEZE SCENT | the avon company canada limited | 02230442 | Lotion - Topical | 17.5 % | 4/3/1997 |
| ARRID XX ULTRA CLEAR SPRAY | carter-horner corp. | 02231609 | Aerosol - Topical | 10 % | 11/28/1997 |
| ARRID EXTRA DRY REG SPRAY 10% | carter products, division of carter wallace ns inc. | 00843032 | Aerosol - Topical | 10 % | 12/31/1989 |
| AVON ROLL ON ANTIPERSP DEOD | the avon company canada limited | 00803650 | Lotion - Topical | 17.5 % | 12/31/1990 |
| ALYSSA ASHLEY MUSK CREME DES.A. BILLE-20 | houbigant (1995) ltée. | 02209683 | Cream - Topical | 20.06 % | 6/27/1996 |
| TABAC ORIGINAL ANTIPERSPIRANT | maurer and wirtz | 00310948 | Aerosol - Topical | .96 % | 12/31/1974 |
| NEO-MEDROL ACNE LOTION | 00195057 | Lotion - Topical | 100 MG / ML | 12/31/1965 | |
| ARRID EXTRA DRY REGULAR SCENT ROLL-ON LOT 20% | carter products, division of carter wallace ns inc. | 00894001 | Lotion - Topical | 20 % | 12/31/1991 |
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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