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Proandre by Proandre SL

Medically reviewed on June 20, 2017

Dosage form: aerosol, foam
Ingredients: ALCOHOL 40mg in 1mL
Labeler: Proandre SL
NDC Code: 70028-003

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.

Antibacterial Handsanitizer Foam

Active Ingredient

Active Ingredient Purpose

Alcohol Denat 68%............ Antibacterial

Uses

Uses

* Hand Sanitizer to help reduce bacteria that potentially may cause disease

Warnings

For external use only

Flammable. Keep away from fire or flame

When using this product

* Avoid contact with face, eyes and broken skin.

If eye contact occurs, flush thoroughly with water

and seek medical advice.

Stop use and ask a doctor if

Stop use and ask a doctor if

* Irritation and redness develops

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help

or contact a Poison Control Center right away.

Directions

Directions

* Pump liquid into dry hands, wet thoroughly and rub

into skin until dry.

* Children under 6 years of age should be supervised by an

adult when using this product.

Inactive Ingredients

Water, Cocamidopropyl betaine

Questions?

Questions?

1(305) 961 1156

Uses

Hand sanitizer to help reduce bacteria on hands. Avoid

contact with broken skin

Antibacterial Hand Sanitizer Foam

Antibacterial Hand Sanitizer Foam

Fragrance Free

PROANDRE 
alcohol denat aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70028-003
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
COCAMIDOPROPYL BETAINE10 mg  in 1 mL
WATER50 mg  in 1 mL
Packaging
#Item CodePackage Description
1NDC:70028-003-11800 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/20/2017
Labeler - Proandre SL (463207675)
Registrant - Proandre SL (463207675)
Establishment
NameAddressID/FEIOperations
Proandre SL463207675manufacture(70028-003)

 
Proandre SL

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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