Sulfur Facial Wash

Manufacturer
GRISI Hnos, S.A DE C.V
Effective date
2025-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:42:45

Label at a glance#

ProductSulfur Facial Wash Acne Cleanser
Active ingredientSULFUR
Label structure12 sections

Indications and uses

■ For the treatment of acne, helps clear up acne pimples/Para el tratamiento del acne, ayuda e eliminar espinillas del acne

Dosage and administration

■ Clean the skin thoroughly before applying this product/Limpiar bien la piel antes de aplicar el producto. ■ Wet affected area with warm water/Humedecer la zona afectada con aqua tibia. ■ Cover the entire affected area with a thin layer and massage until obtaining abundant lather. Leave for 1 minute and rinse thoroughly; one to three times a day/Cubrir el area afectada con una capa delgada y masajear hasta obtene...

Label contents#

Full prescribing information#

Active Ingredients/Ingredientes activos

OTC - ACTIVE INGREDIENT SECTION

Sulfur/Azufre3%

Purpose/Utilidad

OTC - PURPOSE SECTION

Acne treatment/Tratamiento para el acné

Uses/Usos

INDICATIONS & USAGE SECTION

■ For the treatment of acne, helps clear up acne pimples/Para el tratamiento del acne, ayuda e eliminar espinillas del acne

Warnings/Precauciones

WARNINGS SECTION

■ For external use only/Solo par uso externo

■ Not for children under 12 years/No par ninos menores de 12 anos

Do not use/No user en

OTC - DO NOT USE SECTION

■ Broken skin/Heridas abiertas ■ Large areas of the skin/Grandes superficies de piel

When using this product/Cuando use este producto

OTC - WHEN USING SECTION

■ Avoid contact with the eyes. If product gets in the eyes rinse with water/Evire el contacto con los ojos. Si el producto entra en contacto con los ojos, enjuague con agua.
■ Apply only to the areas with acne/Aplique únicamente en áreas con acné

St op use and ask a doctor if/Suspenda su uso y consulte al medico si

OTC - STOP USE SECTION

■ if skin irritation occurs or gets worse, stop use and consult a physician/Aparece alguna irritacion en la piel o esta empeora, suspenda su uso y consulte a su medico.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Mantengase fuera del alcance de los ninos

Directions/Modo de uso

DOSAGE & ADMINISTRATION SECTION

■ Clean the skin thoroughly before applying this product/Limpiar bien la piel antes de aplicar el producto. ■ Wet affected area with warm water/Humedecer la zona afectada con aqua tibia.

■ Cover the entire affected area with a thin layer and massage until obtaining abundant lather. Leave for 1 minute and rinse thoroughly; one to three times a day/Cubrir el area afectada con una capa delgada y masajear hasta obtener espuma. Deja actuar por 1 minuto y enjuagar cuidadosamente; repetir de una a tres veces al dia ■ Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor/Debido a que puede ocurrir un exceso de resequedad en la piel, comience con una aplicación al día e incremente de los a tres veces al dia cuando sea necesario o segun las indicaciones del médico

■ If bothersome dryness or peeling occurs, reduce application to once a day or every other day/Si aparece alguna resequedad o descamación, reduzca la aplicación a una vez al día o cada dos días

Inactive Ingredients/Ingredientes inactivos

INACTIVE INGREDIENT SECTION

Acrylates Copolymer, Aminomethyl Propanol, Caprylyl Glycol, Cocamide MEA, Cocamidopropyl Betaine, Coco-Betaine, Decylene Glycol, Fragrance, Glycerin, Glycol Distearate, Laureth-10, Lauroyl/Myristoyl Methyl Glucamide, Limonene, Linalool, PEG-150, Phenoxyethanol, Polyquaternium-7, Polysorbate 80, Sodium Chloride, Sodium Laureth Sulfate, Tetrasodium EDTA, Water

Questions or comments/Dudas o comentarios

SPL UNCLASSIFIED SECTION

1-833-794-3320

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68437-01268437-012-84

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2abcddde-f15d-f7df-e063-6294a90a0f988d6dfaf2-92ac-9a34-e053-2a95a90a9ca42025-01-14WarningsExact identifier
spl id: 2abcddde-f15d-f7df-e063-6294a90a0f98
spl set id: 8d6dfaf2-92ac-9a34-e053-2a95a90a9ca4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.