HUMPHREYS BENDITO ALCOHOLADO- menthol liquid

Humphreys Bendito Alcoholado by

Drug Labeling and Warnings

Humphreys Bendito Alcoholado by is a Otc medication manufactured, distributed, or labeled by Humphreys Pharmacal, Incorporated, American Distilling Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

DO NOT USE

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.

KEEP OUT OF REACH OF CHILDREN

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

USER SAFETY WARNINGS

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

QUESTIONS

Distribuido por / Dist. by:

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

www.humphreysusa.com

PRINCIPAL DISPLAY PANEL

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

HUMPHREYS

BENDITO
ALCOHOLADO

Analgesia Tópica   /   Topical Anaglesic

REFRESCA - CALMA - PENETRA

INGREDIENTS AND APPEARANCE

HUMPHREYS BENDITO ALCOHOLADO  
menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0219-0203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
menthol (UNII: L7T10EIP3A) (menthol - UNII:L7T10EIP3A)	menthol	12.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Camphor (Synthetic) (UNII: 5TJD82A1ET)
eucalyptol (UNII: RV6J6604TK)
FD&C Blue No. 1 (UNII: H3R47K3TBD)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
isopropyl alcohol (UNII: ND2M416302)
methyl salicylate (UNII: LAV5U5022Y)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0219-0203-80	237 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/11/1972

Labeler - Humphreys Pharmacal, Incorporated (124620340)