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Hydrosal Professional

Dosage form: gel
Ingredients: Aluminum Chloride 15g in 100mL
Labeler: Valeo Pharma Corp.
NDC Code: 30707-100

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Hydrosal Professional

Drug Facts

Aluminum Chloride (Hexahydrate)

15% w/w .......... Antiperspirant

Ask your doctor before use if you have kidney disease.


Do not use on broken, irritated or recently shaved skin.


Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.


If pregnant or breast-feeding, ask a health professional before use.


Decreases underarm perspiration.

Call week days 9AM to 5PM EST at 1 866-694-0150 or visit us at


Stop use if rash, irritation or allergic response occurs.


When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.


apply to underarms only

Other information

Do not use if bottle seal under cap is broken or missing

Keep bottle tightly closed to maintain product properties

Store at 15-250 C (59-770 F)

For external use only

apply a small quantity of product to underarms at bedtime

Inactive ingredients

Alcohol denat., Diazolidinyl Urea (and) Iodopropynyl Butylcarbamate, Disodium EDTA, Ethoxydiglycol, Polyquaternium-10, Purified Water, Salicylic Acid.

aluminum chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30707-100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Chloride (Aluminum cation) Aluminum Chloride15 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Alcohol7 g  in 100 mL
Diazolidinyl urea0.65 g  in 100 mL
Edetate disodium0.2 g  in 100 mL
Diethylene glycol monoethyl ether20 g  in 100 mL
Polyquaternium-10 (400 CPS at 2%)1.75 g  in 100 mL
Water53.4 g  in 100 mL
Salicylic acid2 g  in 100 mL
#Item CodePackage Description
1NDC:30707-100-011 BOTTLE, PLASTIC (BOX) in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35010/01/2007
Labeler - Valeo Pharma Corp. (968337001)
Registrant - Valeo Pharma Corp. (968337001)
Entreprises Importfab Inc.248586117manufacture

Revised: 11/2011
Valeo Pharma Corp.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.