Easment Itch Defense Sulfur Cream-178

Manufacturer
Easment LLC
Effective date
2026-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:38:26

Label at a glance#

ProductEasment Itch Defense Sulfur Cream
Active ingredientSULFUR
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sulfur 1X HPUS

OTC - PURPOSE SECTION

Mite Symptom Relief

DOSAGE & ADMINISTRATION SECTION

  • Temporarily relieves itching and skin discomfort associated with mite exposure.
  • Temporarily relieves itching due to bug bites and minor skin irritation.

WARNINGS SECTION

  • For external use only.
  • Ask a doctor before use if pregnant or nursing.
  • When using this product, avoid contact with eyes, mouth, and mucous membranes.
  • Stop use and ask a doctor if irritation, rash, or worsening symptoms occur, or if symptoms persist for more than 7 days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

INDICATIONS & USAGE SECTION

  • Cleanse and dry the affected area before use.
  • Apply a thin layer to theaffected area 1-3 times daily or as needed.
  • If excessive dryness occurs,reduce frequency of application or discontinue use.
  • Children under 2 years:ask a doctor.

OTHER SAFETY INFORMATION

  • Store at 20-25°C (68-77°F)
  • Protect from excessive heat and sunlight

INACTIVE INGREDIENT SECTION

Aqua, Dipropylene Glycol, Butylene Glycol, Cetearyl Alcohol, Isononyl Isononanoate, Palmitic Acid, Stearic Acid, Glycerin, Dimethicone, Polysorbate 60,PEG-100 Stearate, Glyceryl Stearate, Fomes Officinalis (Mushroom) Extract,1,2-Hexanediol, Hydroxyacetophenone, Polyacrylate Crosspolymer-6, Sorbitan Stearate, Dipotassium Glycyrrhizate, Pentylene Glycol, Lactobacillus/SoymilkFerment Filtrate, Pelargonium Graveolens Flower Oil, Potassium Cetyl Phosphate,Arginine, Butyrospermum Parkii (Shea) Butter, Sophora Flavescens Root Extract,Tribulus Terrestris Fruit Extract, Cornus Officinalis Fruit Extract, Hydroxyphenyl Propamidobenzoic Acid, Pentaerythrityl Tetra-Di-t-Butyl Hydroxyhydrocinnamate,Disodium EDTA, Pandanus Amaryllifolius Leaf Extract, Propanediol, Ascorbyl Palmitate, Ethylhexylglycerin.

OTC - QUESTIONS SECTION

service@easmentllc.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860011972136GTIN-13: 0860011972136
EAN-13: 0860011972136
GTIN-12: 860011972136
UPC-A: 860011972136
GTIN storage (14 digits): 00860011972136
package.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87352-003-01Easment Itch Defense Sulfur Cream60 g in 1 CARTONCREAM601

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87352-00387352-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
Easment Itch Defense Sulfur CreamSULFUR 1X HPUSEasment LLC4f140a93-dc32-0876-e063-6294a90a722a2026-04-09WarningsExact identifier
ndc (package): 87352-003-01
ndc (product): 87352-003
ndc11 (package): 87352000301
spl id: 4f140a93-dc33-0876-e063-6294a90a722a
spl set id: 4f140a93-dc32-0876-e063-6294a90a722a

Reported adverse events (FAERS/openFDA)#

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