ANTIBACTERIAL HAND REFILL- pmcx soap

Antibacterial Hand Refill by

Drug Labeling and Warnings

Antibacterial Hand Refill by is a Otc medication manufactured, distributed, or labeled by Essendant Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient / Ingrediente activo

Chloroxylenol 0.1% / Cloroxilenol al 0.1%

Purpose / Función

Antiseptic / Antiséptico

Uses / Usos

 Handwash to help decrease bacteria on the skin. / Lavado de manos para disminuir las bacterias en la piel.

Warnings / Advertencias

For external use only. / Solo para uso externo.

When using this product / Al utilizar este producto

 Do not use in the eyes. In case of contact, immediately flush eyes with water. / No lo use en los ojos. En caso de contacto, lávese inmediatamente los ojos con agua.

ASK DOCTOR

Stop use and ask a doctor / Suspenda su uso y consulte a un médico
 If irritation or rash develops. / Si aparece y persiste una irritación o sarpullido.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. / Mantener fuera del alcance de los niños.
If swallowed, get medical help or contact a Poison Control Center right away. / En caso de ingestión, busque asistencia médica o contáctese con un centro de toxicología de inmediato.

Directions / Instrucciones

 Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly. / Aplique una pequeña cantidad de producto en las manos mojadas, haga espuma durante 30 segundos y enjuague por completo.
 Children under 6 years of age should be supervised when using this product. / Los niños menores de 6 años deben ser supervisados por un adulto cuando usen este producto.

Inactive ingredients / Ingredientes inactivos

Water (Agua) (7732-18-5), Sodium C14-16 Olefin Sulfonate (Sulfonato de olefina C14-16 de sodio) (68439-57-6), Cocamidopropyl Hydroxysultaine (Cocamidopropil hidroxisultaína) (68139-30-0), Sodium Chloride (Cloruro de sodio) (7647-14-5), Propanediol (Propanodiol) (26264-14-2), Propylene Glycol (Propilenglicol) (57-55-6), Sodium Polyitaconate (Politaconato de sodio) (26099-89-8), Fragrance (Proprietary) (Fragancia (Propietaria)), 2-Bromo-2-Nitropropane-1,3-Diol (-bromo-2-nitropropano-1,3-diol) (52-51-7), Methylisothiazolinone (Metilisotiazolinona) (2682-20-4), Methylchloroisothiazolinone (Metilcloroisotiazolinona) (26172-55-4), Dibromocyanoacetamide (Dibromocianoacetamida) (10222-01-2), Yellow 5 (Amarillo 5) (1934-21-0), Red 40 (Rojo 40) (25956-17-6).

Other Information / Otra información

 Store below 104°F (40°C). May discolor certain fabrics or surfaces. / Almacenar por debajo 104°F (40°C). Puede decolorar ciertas telas o superficies.

Questions? / ¿Preguntas?

 1-844-828-5617

Package Label

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND REFILL 
pmcx soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71906-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	1 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FD&C RED NO. 40 (UNII: WZB9127XOA)
PROPANEDIOL (UNII: 5965N8W85T)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
WATER (UNII: 059QF0KO0R)
CINNAMALDEHYDE (UNII: SR60A3XG0F)
EUGENOL (UNII: 3T8H1794QW)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED) (UNII: G7SW5QN7TT)
DIBROMOCYANOACETAMIDE (UNII: 7N51QGL6MJ)
BRONOPOL (UNII: 6PU1E16C9W)

Product Characteristics
Color	orange (Clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71906-701-41	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/11/2022

Labeler - Essendant Co. (007981038)