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BACTEX Antiseptic Hand Sanitizer

Dosage form: gel
Ingredients: ALCOHOL 62mL in 100mL
Labeler: Punto Rojo, S.A
NDC Code: 49839-200

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.

BACTEX Antibacterial Antiseptic Hand Sanitizer

Drug Facts

Active Ingredient                                Purpose

Ethyl Alcohol 62 percent                  Antimicrobial

Uses for hand washing to decrease bacteria on the skin.

Warnings

Flammable, keep away from fire or flame

For external use only

Do not use in the eyes

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of the reach of children.

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

Directions:

Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients:

Deionized water, Propylene Glycol, Glycerol Ethoxylate, Triethanolamine

Questions or Comments

Call: 506 2442 04848

Write to: Departamento de Mercadeo

Apartado 344-4050 Alajuela, Costa Rica

www.puntorojo.com

Email: informacion@puntorojo.com

Manufactured By:

Punto Rojo S.A.

200 Metros Norte de

los Tribunales de Justicia

Alajuela, 160-4050

Costa Rica


BACTEX
Antibacterial

Antiseptic
Hand Sanitizer

NO WATER REQUIRED 
FAST ACTING

Product Of Costa Rica

Kills 99.9 percent of Germs

Net Contents 2.7 Oz.

BACTEX ANTISEPTIC HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49839-200
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
TROLAMINE 
Packaging
#Item CodePackage Description
1NDC:49839-200-1080 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33311/01/2009
Labeler - Punto Rojo, S.A (853018687)
Registrant - Punto Rojo, S.A (853018687)
Establishment
NameAddressID/FEIOperations
Punto Rojo, S.A853018687manufacture

 
Punto Rojo, S.A

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Medically reviewed on Oct 2, 2018

Further information

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

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