Inactive Ingredients

Manufacturer
Laboratorio Neo Farmaco del Ecuador Neofarmaco Cia. LTDA.
Effective date
2026-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-23 05:10:05

Label at a glance#

ProductJabon Sulfuroso del Dr Pena
Active ingredientSULFUR, POVIDONE-IODINE, CAMPHOR, (-)-, METHYL SALICYLATE
Label structure10 sections

Dosage and administration

Wet affected area • Apply product and massage gently • Rinse thoroughly • Use one to three times daily • Because excessive drying of the skin may occur, start with one application daily, then gradually increase if needed • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Label contents#

Full prescribing information#

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hydrogenated Palm Kernel Oil, Sodium Hydroxide, Water

(Aqua), Fragrance (Parfum), Titanium Dioxide (CI 77891),

Yellow 10 Lake (CI 47005)

Directions

INSTRUCTIONS FOR USE SECTION

Wet affected area

• Apply product and massage gently

• Rinse thoroughly

• Use one to three times daily

• Because excessive drying of the skin may occur, start with

one application daily, then gradually increase if needed

• If bothersome dryness or peeling occurs, reduce

application to once a day or every other day

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - Sulfur 3%Active Ingredients - Sulfur 3%Sulfur 3% .....….......................................... Acne Treatment

DOSAGE & ADMINISTRATION SECTION

Directions

• Wet affected area

• Apply product and massage gently

• Rinse thoroughly

• Use one to three times daily

• Because excessive drying of the skin may occur, start with

one application daily, then gradually increase if needed

• If bothersome dryness or peeling occurs, reduce

application to once a day or every other day

WARNINGS SECTION

Warnings

•For external use only

•When using this product Avoid contact with eyes. Skin

irritation and dryness are more likely to occur if you use

another topical acne medication at the same time. If irritation

occurs, use only one topical acne medication at a time

•Stop use and ask a doctor Excessive irritation develops or

increases

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out reach of children

If product is swallowed, get medical help of contact a Poison

Control Center right away

OTC - PURPOSE SECTION

Uses

Helps treat acne, Helps prevent new acne pimples, Cleanses oily skin

INDICATIONS & USAGE SECTION

Indication and UsesIndication and Uses

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel Jabon SulfurosoPrincipal Display Panel Jabon SulfurosoPDP - Jabon Sulfuroso

YODO SALIL PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP YODO SALILPDP YODO SALIL

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87845-10287845-102-01
87845-10187845-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-07-13daily-update2026-07-18 05:11:06

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
Yodo SalilOINTMENTLaboratorio Neo Farmaco del Ecuador Neofarmaco Cia. LTDA.56812625-7eab-6a25-e063-6294a90a23fe2026-07-20WarningsExact identifier
ndc (package): 87845-101-01
ndc (package): 87845-102-01
ndc (product): 87845-102
ndc (product): 87845-101
ndc11 (package): 87845010201
ndc11 (package): 87845010101
spl id: 570cf5f1-da9e-717d-e063-6394a90aec92
spl set id: 56812625-7eab-6a25-e063-6294a90a23fe

Reported adverse events (FAERS/openFDA)#

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