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Over-the-counter medicine · no prescription needed

Aluminum chlorohydrate anhydrous

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 chlorohydrate anhydrous used for?
The Drug Facts label of Old Spice Oasis with Vanilla Notes Dry (The Procter & Gamble Manufacturing Company) lists these uses: reduces underarm wetness.
Do I need a prescription for Aluminum chlorohydrate anhydrous?
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 chlorohydrate anhydrous 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.

Old Spice Oasis with Vanilla Notes Dry · The Procter & Gamble Manufacturing Company

Aluminum chlorohydrate anhydrous 24.5%, aerosol, spray (topical)

Active ingredient

Aluminum chlorohydrate 24.5.0% (anhydrous)

Purpose

Antiperspirant

Uses

reduces underarm wetness

Warnings

For external use only.

Do not use

on broken skin

Ask a doctor before use if

you have kidney disease Stop use if rash or irritation occurs

Keep out of reach of children

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

When using this product

keep away from face and mouth to avoid breathing it avoid spraying in eyes use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Directions

apply to underarms only

Inactive ingredients

Butane, hydrofluorocarbon 152A, dimethicone, C12-15 alkyl benzoate, isopropyl myristate, PPG-14 butyl ether, fragrance, disteardimonium hectorite, mineral oil, propylene carbonate, corn starch/maltodextrin crosspolymer, dimethiconol

Questions?

1-800-677-7582

— FDA label of Old Spice Oasis with Vanilla Notes Dry, The Procter & Gamble Manufacturing Company, effective December 31, 2025. See the official label on DailyMed →

Sure Regular Antiperspirant and Deodorant · Sodalis USA LLC

Aluminum chlorohydrate anhydrous 10%, aerosol, spray (topical)

Active ingredient

Aluminum Chlorohydrate 10% (anhydrous) Purpose Antiperspirant

Purpose

Antiperspirant

Uses

reduces underarm wetness

Warnings

For external use only. Flammable do not spray near flame or while smoking contents under pressure do not crush, puncture or incinerate do not store at temperature above 120ºF

Do not use

on broken skin

Ask a doctor before use if

you have kidney disease

When using this product

keep away from face and mouth to avoid breathing it avoid spraying in eyes use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal Stop use if rash or irritation occurs

Keep out of reach of children

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

Directions

apply to underarms only shake well before each use hold can about 6 inches away from underarm and spray.

Inactive ingredients

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Aluminum Chlorohydrate, Isopropyl Palmitate, Dimethicone, Disteardimonium Hectorite, Propylene Carbonate, Fragrance (Parfum), Amyl cinnamal, Benzyl alcohol, Cinnamyl alcohol, Citral, Eugenol, Isoeugenol, Amylcin-namyl alcohol, Coumarin, Geraniol, Benzyl cinnamate, Linalool, Benzyl benzoate, Citronellol, Hexyl cinnam-aldehyde, d-Limonene.

Questions?

1-800-575-7960 www.suredeodorant.com

— FDA label of Sure Regular Antiperspirant and Deodorant, Sodalis USA LLC, effective November 8, 2024. See the official label on DailyMed →

Antitranspirante Above Rollon Extreme Black · Baston Industria De Aerossois Ltda

Aluminum chlorohydrate anhydrous 12 mg/50 mL, cream (topical)

Active ingredient

ALUMINUM CHLOROHYDRATE 12% ALUMINUM CHLOROHYDRATE 12%

Purpose

ALUMINUM CHLOROHYDRATE ANTIPERSPIRANT ALUMINUM CHLOROHYDRATE ANTIPERSPIRANT

Uses

only on the armpits. Wait for it to dry before getting dressed. Do not apply to wet skin. Apply only to the underarms. Use only on the armpits. Wait for it to dry before getting dressed. Do not apply to wet skin. Apply only to the underarms.

Warnings

Use only in the indicated areas.

Do not use

if the skin is irritated or injured. If irritation and/or itching occurs at the application site, discontinue use immediately and seek medical advice.

Keep out of reach of children

and pets. Store in a dry place at room temperature with the cap closed. See packaging for batch number and expiry date. Use only in the indicated areas.

Do not use

if the skin is irritated or injured. If irritation and/or itching occurs at the application site, discontinue use immediately and seek medical advice.

Keep out of reach of children

and pets. Store in a dry place at room temperature with the cap closed. See packaging for batch number and expiry date. KEEP OUT OF REACH OF CHILDREN KEEP OUT OF REACH OF CHILDREN

Directions

UNDERARM ANTIPERSPIRANT DEODORANT UNDERARM ANTIPERSPIRANT DEODORANT

Inactive ingredients

AQUA, ALUMINUM CHLOROHYDRATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, STEARETH-2, GLYCINE, CALCIUM CHLORIDE, STEARETH-21, SILICA, ACRYLATES COPOLYMER, CETEARETH-20, 2-METHYL-5-CYCLOHEXYLPENTANOL, MORINGA OLEIFERA SEED OIL, ACRYLATES, C10-30 ALKYL ACRYLATE CROSSPOLYMER, MALTODEXTRIN, CITRIC ACID, SODIUM GLUCONATE, GOSSYPIUM HERBACEUM SEED OIL, SODIUM LAURETH SULFATE, BUTYROSPERMUM PARKII BUTTER, MACADAMIA TERNIFOLIA SEED OIL, COCOS NUCIFERA FRUIT EXTRACT, CHAMOMILLA RECUTITA FLOWER EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, CINNAMOMUM ZEYLANICUM BARK EXTRACT, ACORUS CALAMUS ROOT EXTRACT, COMMIPHORA MYRRHA RESIN EXTRACT, OLEA EUROPAEA FRUIT OIL, ARGANIA SPINOSA KERNEL OIL, LECITHIN, POLYGLYCERYL-3 DIISOSTEARATE, GLYCERIN, GLYCERYL STEARATE, SILVER, GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE, PARFUM, BENZYL SALICYLATE, COUMARIN, LINALOOL, HYDROXYCITRONELLAL, GERANIOL, ALPHA-ISOMETHYL IONONE, CITRAL, LIMONENE AQUA, ALUMINUM CHLOROHYDRATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, STEARETH-2, GLYCINE, CALCIUM CHLORIDE, STEARETH-21, SILICA, ACRYLATES COPOLYMER, CETEARETH-20, 2-METHYL-5-CYCLOHEXYLPENTANOL, MORINGA OLEIFERA SEED OIL, ACRYLATES, C10-30 ALKYL ACRYLATE CROSSPOLYMER, MALTODEXTRIN, CITRIC ACID, SODIUM GLUCONATE, GOSSYPIUM HERBACEUM SEED OIL, SODIUM LAURETH SULFATE, BUTYROSPERMUM PARKII BUTTER, MACADAMIA TERNIFOLIA SEED OIL, COCOS NUCIFERA FRUIT EXTRACT, CHAMOMILLA RECUTITA FLOWER EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, CINNAMOMUM ZEYLANICUM BARK EXTRACT, ACORUS CALAMUS ROOT EXTRACT, COMMIPHORA MYRRHA RESIN EXTRACT, OLEA EUROPAEA FRUIT OIL, ARGANIA SPINOSA KERNEL OIL, LECITHIN, POLYGLYCERYL-3 DIISOSTEARATE, GLYCERIN, GLYCERYL STEARATE, SILVER, GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE, PARFUM, BENZYL SALICYLATE, COUMARIN, LINALOOL, HYDROXYCITRONELLAL, GERANIOL, ALPHA-ISOMETHYL IONONE, CITRAL, LIMONENE

Questions?

SUPPORT@MYSPRAY.GROUP OR CALL (305) 766-5030 SUPPORT@MYSPRAY.GROUP OR CALL (305) 766-5030

— FDA label of Antitranspirante Above Rollon Extreme Black, Baston Industria De Aerossois Ltda, effective February 18, 2026. See the official label on DailyMed →

MDS Roll-On Anti-Perspirant · Mds Global Fze

Aluminum chlorohydrate anhydrous 15.4%, cream (topical)

Active ingredient

Aluminum Chlorohydrate, 15.4 % anhydrous

Purpose

Anti-Perspirant Deodorant

Uses

reduces underarm perspiration

Warnings

For external use only Do not apply to broken 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 a Poison Control Center right away.

Directions

apply to underarms only

Inactive ingredients

DIMETHICONOL, FRAGRANCE, ISOPROPYL MYRISTATE, STEARETH-2, STEARETH-20, WATER.

— FDA label of MDS Roll-On Anti-Perspirant, Mds Global Fze, effective November 10, 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 chlorohydrate anhydrous 24.5% · aerosol, spray (topical) · 12 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Gillette Dryshield Arctic Ice Dry The Procter & Gamble Manufacturing Company DailyMed
Gillette Dryshield Cool Wave Dry The Procter & Gamble Manufacturing Company DailyMed
Gillette Dryshield Power Rush Dry The Procter & Gamble Manufacturing Company DailyMed
Old Spice Co ld Spice Scent of Cool Mint Dry The Procter & Gamble Manufacturing Company DailyMed
Old Spice Fresh High Endurance Dry The Procter & Gamble Manufacturing Company DailyMed
Old Spice Oasis with Vanilla Notes Dry The Procter & Gamble Manufacturing Company DailyMed
Old Spice Pure Sport Scent of Citrus Zest Dry The Procter & Gamble Manufacturing Company DailyMed
Secret Original Dry Powder Fresh The Procter & Gamble Manufacturing Company DailyMed
Secret Original Dry Shower Fresh The Procter & Gamble Manufacturing Company DailyMed
Secret Outlast Dry Completely Clean The Procter & Gamble Manufacturing Company DailyMed
Secret Outlast Dry Protecting Powder The Procter & Gamble Manufacturing Company DailyMed
Secret Weightless Dry Brown Sugar plus Argan Oil The Procter & Gamble Manufacturing Company DailyMed
Aluminum chlorohydrate anhydrous 10% · aerosol, spray (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Sure Regular Antiperspirant and Deodorant Sodalis USA LLC DailyMed
Sure Unscented Antiperspirant and Deodorant Sodalis USA LLC DailyMed
Aluminum chlorohydrate anhydrous 12 mg/50 mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Antitranspirante Above Rollon Extreme Black Baston Industria De Aerossois Ltda DailyMed
Aluminum chlorohydrate anhydrous 15.4% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
MDS Roll-On Anti-Perspirant Mds Global Fze DailyMed

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.

  • The Procter & Gamble Manufacturing Company12 products
  • Sodalis USA LLC2 products
  • Baston Industria De Aerossois Ltda1 product
  • Mds Global Fze1 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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