Medication Guide App

Lactovit Men Roll-On Antiperspirant Deodorant

Dosage form: liquid
Ingredients: ALUMINUM CHLOROHYDRATE 15mL in 100mL
Labeler: Antonio Puig, S.A.
NDC Code: 50007-3000

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.

Lactovit Men - Aluminum Chlorohydrate

Active Ingredient

Aluminum Chlorohydrate 15 percent

Purpose

Antiperspirant

Uses

- Reduces underarm wetness.

Directions

- Apply to underarms only.

- For external use only.

- Do not use on broken skin.

- Stop use if rash or irritation occurs.

- Ask a doctor before using if you have kidney disease.

- Keep out of reach of children. If swallowed, get medical help or
  contact Poison Control Center right away.

Other Information:

Store at room temperature.

Inactive Ingredients

Acetyl Dipeptide-3 Amino-hexanoate, Allantoin, Ascorbic Acid, BHT,

Butylene Glycol, Cyclopentasiloxane, Edetate Disodium, Fragrance,

Hydrolyzed Milk Protein, Phenoxyethanol, Povidone/Eicosene Copolymer,

PPG-15 Stearyl Ether, Propyl Gallate, Spirulina Platensis Extract, Steareth-2,

Steareth-21, Triclosan, Water

Manufactured by:

Antonio Puig S.A.

Travessera de Gracia, 9

Barcelona E-08021

Spain

Made in Spain

LACTOVIT MEN ROLL-ON ANTIPERSPIRANT DEODORANT 
aluminum chlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50007-3000
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CATION) ALUMINUM CHLOROHYDRATE15 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN 
ASCORBIC ACID 
BUTYLATED HYDROXYTOLUENE 
BUTYLENE GLYCOL 
CYCLOMETHICONE 5 
EDETATE DISODIUM 
PHENOXYETHANOL 
PROPYL GALLATE 
TRICLOSAN 
WATER 
Packaging
#Item CodePackage Description
1NDC:50007-3000-150 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35012/16/2009
Labeler - Antonio Puig, S.A. (460013279)
Registrant - Antonio Puig, S.A. (460013279)
Establishment
NameAddressID/FEIOperations
Antonio Puig, S.A.460013279manufacture

Revised: 12/2009
 
Antonio Puig, S.A.

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.

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