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Humphreys Bendito Alcoholado

Dosage form: liquid
Ingredients: menthol 12.5mg in 1mL
Labeler: Humphreys Pharmacal, Incorporated
NDC Code: 0219-0203

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.

Monografía / Drug Facts

Ingrediente activo / Active ingredients

Mentol / Menthol 1.25%

Propósito / Purpose

Analgesia Tópica / Topical Anaglesic

Usos / Uses

Para un alivio temporal de dolores musculares y dolores en las articulaciones asociados con:

  • artritis
  • moretones
  • esguinces
  • tensión
  • achaques de espalda
For the temporary relief of minor aches and pains of muscles and joints associated with:
  • arthritis
  • bruises
  • sprains
  • strains
  • simple backache

Advertencias / Warnings

Para uso externo solamente. Evite el contacto con los ojos o las membranas mucosas. Si la condición empeora o los síntomas persisten por más de 7 dias, o si se aliviany retoman días después, interrumpa el uso del producto y consulte a un médico.

For external use only. Avoid contact with eyes or mucous membranes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

No use este producto si su piel es sensible al aceite de menta-verde (salicilato de metilo). No aplique a heridas ni a la piel maltratada. No ponga un vendaje muy apretado.
Do not use if skin is sensitive to oil of wintergreen (methylsalicylate). Do not apply to wounds or damaged skin. Do not bandage tightly.

Mantenga fuera del alcance de niños. Si se ingiere, consiga asistencia médica o llame al Centro de Control de Venenos inmediatamente.
Keep out of the reach of children. If swallowed,get medical help or contact a Poison Control Center right away

Inflamable. Mantenga alejado del fuego, chispas y superficies calientes.
Flammable keep away from fire, sparks and heated surfaces.

Instrucciones / Directions

Adultos y niños de 2 años en adelante: Aplique sobre la zona afectada no más de 3 ó 4 veces al dia. Niños menores de 2 años en edad: consulte a un médico.
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Ingredientes inactivos / Inactive ingredients

camphor, eucalyptol, FDC blue #1, FDC yellow #5, isopropyl alcohol, methyl salicylate, and purified water

Otra información / Other information

Almacene debajo de 30C / Store below 86F

Distribuido por / Dist. by:

Humphreys Pharmacal, Inc.
East Hampton, CT 06424
Made in USA

The labels shown below represent a sample of that currently in use. Additional packaging may also be available.



Analgesia Tópica   /   Topical Anaglesic


menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0219-0203
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
menthol (menthol) menthol12.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Camphor (Synthetic) 
FD&C Blue No. 1 
FD&C Yellow No. 5 
isopropyl alcohol 
methyl salicylate 
#Item CodePackage Description
1NDC:0219-0203-80237 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/11/1972
Labeler - Humphreys Pharmacal, Incorporated (124620340)

Humphreys Pharmacal, Incorporated

Medically reviewed on Mar 5, 2018

Further information

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