Over-the-counter medicine
Aluminum chlorohydrate
Aluminum chlorohydrate is an over-the-counter medicine. No generic is listed in FDA's NDC Directory.
- No generic listed
- Over the counter
Check it at the source: the aluminum chlorohydrate FDA label on DailyMed (effective February 9, 2026); every aluminum chlorohydrate label on DailyMed.
Highlights of the record
FDA label of February 9, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026
Used for
From the label: indications and usagereduces underarm wetness
Forms and strengths
- 0.19 g/g
- 0.25 g/ml
- 7.1 g/71g
- 9.6 mg/100g
- 10 g/100ml
- 12 mg/100g
- 12.3 g/100ml
- 15 g/100g
- 19 g/100g
- 19.6 g/100g
- 20 g/100g
- 20 g/103ml
Aerosol (spray); stick; cream; liquid; spray.
On the market
- Generic approvals
- No generic approved
- Labelers listed (NDC)
- 71 of which 0 under generic applications, 0 under brand applications, repackagers included
Supply and safety
- Pharmacy cost (NADAC)
- Not in the survey
- Shortage (FDA)
- No current entry
- Recalls by its makers (FDA)
- 0 since 2021 1 Class I among all firms' recalls; 2 more by firms not listed as its makers
- FAERS reports
- 40 through July 30, 2026
What is aluminum chlorohydrate used for?
From the label: indications and usagereduces underarm wetness
Source: FDA drug label (Mando Pro Sport), Lume Deodorant, LLC., effective February 9, 2026 (SPL set 47be10c1-61ad-48a8-e063-6294a90a7cb4), via openFDA; the full label on DailyMed
Is there a generic for aluminum chlorohydrate?
No generic aluminum chlorohydrate is approved (Drugs@FDA, October 8, 2026).
Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)
Has aluminum chlorohydrate been recalled?
The FDA's Enforcement Report lists 2 recalls naming aluminum chlorohydrate since 2021: 1 Class I (the most serious), 1 Class II, 0 Class III; 0 still ongoing. 2 of them are by firms that FDA's NDC Directory does not list as a maker of aluminum chlorohydrate and that hold no application for it in Drugs@FDA, such as compounding pharmacies or bulk-ingredient suppliers; the recall notice names the product recalled. A recall names products and lots, not every product of the medicine.
| Started | Class | Company | Reason |
|---|---|---|---|
| November 23, 2021 | Class I | The Procter & Gamble Company not a listed maker | Chemical contamination: presence of benzene |
| November 23, 2021 | Class II | The Procter & Gamble Company not a listed maker | CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene |
Source: FDA Enforcement Report (drug recalls) via openFDA, through October 8, 2026
What do FAERS reports show for aluminum chlorohydrate?
The FDA Adverse Event Reporting System holds 40 reports that list aluminum chlorohydrate among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 3 are coded as a death and 8 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.
The most reported reactions
Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026
What next?
- Aluminum chlorohydrate side effects
- the label's list beside FAERS reports
- Check an interaction
- what two or more labels say about each other