Humphreys Pharmacal, Incorporated

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 ingredient

Alcohol etilico 70% / Ethyl alcohol 70%

Propósito / Purpose

Antiséptico / Antiseptic

Usos / Uses

ayuda primaria para prevenir el riesgo de la infección en:
first aid to help prevent the risk of infection in:

Advertencias / Warnings

Para uso externo solamente. / For external use only.

Inflamable, mantenga lejos de fuego y chispas/ Flammable, keep away from fire or flame

Consulte a un médico antes de usar si usted tiene heridas profundas, una perforación, mordidas de animal o quemaduras graves / Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

Cuando se usa este producto / When using this product

Descontinúe y consulte a un médico si la condición persiste o empeora
Stop use and ask doctor if condition persists or gets worse

Mantenga alejado de los niños. Si se ingiere, busque ayuda médica inmediatamente.
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Direcciones / Directions

Aplique sobre la piel directamente o con una gasa limpia, algodón o un bastoncillo de algodón / Apply to the skin directly or with clean gauze, cotton, or swab

Ingredientes inactivos / Inactive ingredients

bay oil, denatonium benzoate, FDC blue #1, FDC red #40, FDC yellow #5, FDC yellow #6, fragrance, hamamelis virginianna, menthol, polysorbate 20, purified water, t-butyl alcohol

Otra información / Other information

Almacenar por debajo de 30C. Store below 86F.

Distribuido por / Dist. by:

Humphreys Pharmacal, Inc.
East Hampton, CT 06424

Made in USA

Product Packaging

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



Antiseptic Lotion / Loción Anticeptica


Alcoholado label

alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0219-2020
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
bay oil (pimenta racemosa) (UNII: 3T5GC5CQ33)  
denatonium benzoate (UNII: 4YK5Z54AT2)  
fd&c blue no. 1 (UNII: H3R47K3TBD)  
fd&c red no. 40 (UNII: WZB9127XOA)  
fd&c yellow no. 5 (UNII: I753WB2F1M)  
fd&c yellow no. 6 (UNII: H77VEI93A8)  
witch hazel (UNII: 101I4J0U34)  
menthol (UNII: L7T10EIP3A)  
polysorbate 20 (UNII: 7T1F30V5YH)  
water (UNII: 059QF0KO0R)  
tert-butyl alcohol (UNII: MD83SFE959)  
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0219-2020-16 473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/11/1972
Labeler - Humphreys Pharmacal, Incorporated (124620340)

Revised: 2/2013
Document Id: 452b8063-1649-4f06-9b6e-99881ba74453
Set id: 9f629487-1644-4176-bf04-19efc9eaacdc
Version: 1
Effective Time: 20130204
Humphreys Pharmacal, Incorporated