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Over-the-counter medicine · no prescription needed

Aluminum chloride

Purpose on the label: Antiperspirant

Antiperspirants

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Aluminum chloride used for?
The Drug Facts label of Pure Dry (Chongqing Alefa Technology Co., Ltd.) lists these uses: Reduces underarm wetness..
Do I need a prescription for Aluminum chloride?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredient, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Aluminum chloride been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Pure Dry · Chongqing Alefa Technology Co., Ltd.

Aluminum chloride 15%, liquid (topical)

Active ingredient

Aluminum Chloride 15%(9g/60ml)

Purpose

antiperspirant for hands & feet

Uses

Reduces underarm wetness.

Warnings

For external use only.

Do not use

on broken or recently shaved skin. Avoid contact with eyes or mouth. Stop use if irritation or rash occurs.

Keep out of reach of children

Directions

Apply to underarms only. Apply at bedtime to clean, fully dry underarms. Apply sparingly — only a few strokes under each arm. Do not apply immediately after shaving or on irritated skin. For sensitive skin: start 2–3 nights per week, then increase as needed. Let dry before dressing.

Inactive ingredients

Purified Water, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Allantoin, Aloe Barbadensis Leaf Juice Powder

— FDA label of Pure Dry, Chongqing Alefa Technology Co., Ltd., effective April 22, 2026. See the official label on DailyMed →

Certain Dri Antiperspirant Hand-Lotion · Clarion Brands, LLC

Aluminum chloride 0.15%, lotion (topical)

Active ingredient

Aluminum chloride 15%

Purpose

Antiperspirant

Uses

reduces perspiration

Warnings

For external use only

Do not use

on broken or irritated skin immediately after shaving immediately after bathing

Ask a doctor before use if

you have kidney disease

When using this product

do not use in or near eyes

Stop use and ask a doctor if

rash or irritation develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wash and dry hands thoroughly before application apply a small, pea sized amount to the palms of your hands rub into palms vigorously for 15 seconds for best results, apply every night before bed and an additional two times per day for at least four weeks

Inactive ingredients

aloe barbadensis leaf juice, artemisia vulgarixs extract, behentrimonium methosulfate, bisaolol, bis-laurl cocaminopropylamine/HDI/PEG-100 copolymer, butylene glycol, cetearyl alcohol, cetyl alcohol, dimethicone, ethylhexyglycerin, hydroxyethylcellulose, jojoba esters, laminaria digitata extract, opuntia ficus-indica fruit extract, potassium hydroxide, saccharomyces cerevisiae extract, water, zingiber officinale (ginger) root extract

Questions?

call 1-844-923-7837

— FDA label of Certain Dri Antiperspirant Hand-Lotion, Clarion Brands, LLC, effective December 23, 2025. See the official label on DailyMed →

Xerac AC · Person and Covey

Aluminum chloride 6.25%, liquid (topical)

Active ingredient

OTC - ACTIVE INGREDIENT SECTION Aluminum Chloride Hexahydrate

Purpose

OTC - PURPOSE SECTION For topical application as an antiperspirant (anhidrotic).

Uses

Indicatins and Usage Section For patients suffering from hyperhidrosis, or patients whose jobs or sports activities cause excessive sweating that exacerbates other skin problems.

Warnings

SECTION For external use only. Avoid contact with eyes. If contact occurs, wash eyes thoroughly with water. If irritation or sensitization occurs, discontinue use or contact a physician. Xerac AC may be harmful to cotton fibers and certain metals. OTC - KEEP OUT OF REACH OF CHILDREN SECTION Yes. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION Xerac AC when applied to the underarms, should be applied to absolutely dry skin. Only apply Xerac AC before bedtime, since medication should be kept on the skin for 6-8 hours. To reduce irritation, let the alcohol evaporate, leaving a thin film of antiperspirant on the skin. Wear a T-shirt, while sleeping to prevent medication from being rubbed off on the bed linens. Do not apply Xerac AC to broken, irritated or recently shaved skin. Wash the treated area next morning with soap and water. Do not apply other deodorants or antiperspirants while using Xerac AC.

Inactive ingredients

SECTION Anhydrous ethanol

— FDA label of Xerac AC, Person and Covey, effective November 28, 2025. See the official label on DailyMed →

Sweatblock Original Maximum Clinical Protection · DC Alpine Partners, LLC

Aluminum chloride 150 mg/mL, solution (topical)

Active ingredient

Aluminum chloride 15% (Maximum % of Aluminum Chloride allowed by USFDA without a prescription)

Purpose

Antiperspirant

Uses

HOW TO APPLY: 1. Apply at night, before bedtime. 2. Gently press to clean, dry skin (do not rub). 3. Air dry for 5 minutes and go to bed. 4. In the morning, wash the treated area. Uses Reduces excessive sweating Decreases underarm sweating

Warnings

For external use only.

Do not use

on broken or irritated skin. Stop use if rash or irritation occurs.

Ask a doctor before use if

you have kidney disease.

Keep out of reach of children

If swallowed, get medical help or contact Poison Control Center immediately.

Directions

Apply at bedtime. Ensure skin is clean and dry. Use every 7 days, or as needed.

Inactive ingredients

Allantoin, Benzoic Acid, Ethylhexylglycerin, Hamamelis Virginiana (Witch Hazel) Water, Phenoxyethanol, Polysorbate 20, Tocopheryl Acetate (Vitamin E Oil), Water (Aqua)

Questions?

Call Toll Free 1-855-796-2566

— FDA label of Sweatblock Original Maximum Clinical Protection, DC Alpine Partners, LLC, effective June 23, 2026. See the official label on DailyMed →

Certain Dri Roll-On · Clarion Brands, LLC

Aluminum chloride 0.12 mg/mL, liquid (topical)

Purpose

Active ingredient Purpose Aluminum Chloride 12.0% Antiperspirant

Uses

extra effective at reducing underarm perspiration

Warnings

For external use only

Do not use

immediately after shaving on broken skin on irritated skin immediately after bathing

Ask a doctor before use if

you have kidney disease

When using this product

do not use in or near eyes apply to underarms only

Stop use and ask a doctor if

rash or irritation develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

apply to underarms only apply at bedtime, see package insert apply sparingly apply only a few strokes under each arm

Inactive ingredients

polyacrylate crosspolymer-6, sodium hydroxide, water

Questions?

Call 1-844-923-7837

— FDA label of Certain Dri Roll-On, Clarion Brands, LLC, effective December 23, 2025. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredient, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Aluminum chloride 15% · liquid (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Certain Dri Clinical Strength Prescription Protection Rollon Clarion Brands LLC DailyMed
Pure Dry Chongqing Alefa Technology Co., Ltd. DailyMed
Aluminum chloride 0.15% · lotion (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Certain Dri Antiperspirant Foot-Lotion Clarion Brands, LLC DailyMed
Certain Dri Antiperspirant Hand-Lotion Clarion Brands, LLC DailyMed
Aluminum chloride 6.25% · liquid (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Xerac AC Person and Covey DailyMed
Aluminum chloride 150 mg/mL · solution (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Sweatblock Original Maximum Clinical Protection DC Alpine Partners, LLC DailyMed
Aluminum chloride 0.12 mg/mL · liquid (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Certain Dri Roll-On Clarion Brands, LLC DailyMed
Aluminum chloride 0.15% · for solution (topical) · 1 product
Brand or product nameCompany on the labelLabel
Certain Dri Clinical Strength Roll On Clarion Brands, LLC —
Aluminum chloride 15% · spray, metered (topical) · 1 product
Brand or product nameCompany on the labelLabel
Dry Grip Chongqing Alefa Technology Co., Ltd. DailyMed
Aluminum chloride 15% · cream (topical) · 1 product
Brand or product nameCompany on the labelLabel
Hand Antiperspirant Nightly Use Clutch Inc DailyMed
Aluminum chloride 12 mg/mL · liquid (topical) · 1 product
Brand or product nameCompany on the labelLabel
Clinical Strength MiracleDry Antiperspirant Deodorant PM Highland Consumer Products DailyMed
Aluminum chloride 150 mg/mL · gel (topical) · 1 product
Brand or product nameCompany on the labelLabel
Duradry Sweat Minimizing Gel Novadore USA Inc DailyMed

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Aluminum chloride, by strength and form
Strength and formGeneric or brandPharmacies pay
aluminum chloride 6.25%
liquid
Generic $0.1722–$0.2183 per mL
2 packages, lowest to highest

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • Clarion Brands, LLC5 products
  • Chongqing Alefa Technology Co., Ltd.2 products
  • Person and Covey1 product
  • DC Alpine Partners, LLC1 product
  • Clutch Inc1 product
  • Highland Consumer Products1 product
  • Novadore USA Inc1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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