EASMENT ITCH DEFENSE SULFUR CREAM- sulfur 1x hpus cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Sulfur 1X HPUS

PURPOSE

Mite Symptom Relief

DOSAGE & ADMINISTRATION

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

WARNINGS

• 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.

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

INDICATIONS & USAGE

• 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

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.

QUESTIONS

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EASMENT ITCH DEFENSE SULFUR CREAM 
sulfur 1x hpus cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87352-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	1 [hp_X]  in 60 g

Inactive Ingredients
Ingredient Name	Strength
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
POLYSORBATE 60 (UNII: CAL22UVI4M)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
DIMETHICONE (UNII: 92RU3N3Y1O)
AQUA (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PALMITIC ACID (UNII: 2V16EO95H1)
PEG-100 STEARATE (UNII: YD01N1999R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
LACTOBACILLUS (UNII: 5307V7XW8I)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
ARGININE (UNII: 94ZLA3W45F)
PANDANUS AMARYLLIFOLIUS LEAF (UNII: 7TVT2CK45V)
CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN STEARATE (UNII: NVZ4I0H58X)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87352-003-01	60 g in 1 CARTON; Type 0: Not a Combination Product	04/30/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/30/2026

Labeler - Easment LLC (140938573)