Home NDC 87352-006 Easment Itch Defense Sulfur Cream
Product NDC 87352-006
11-digit product format 873520006
Labeler code 87352
Product ID 87352-006_5835f842-6429-0782-e063-6294a90ad182
Type HUMAN OTC DRUG
Nonproprietary name Sulfur 1X HPUS
Dosage form CREAM
Route TOPICAL
Labeler Easment LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-09-04
Substance SULFUR
Active strength 1 [hp_X]/120g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Easment Itch Defense Sulfur Cream
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 1 [hp_X]/120g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87352-006-01 87352000601 120 g in 1 CARTON (87352-006-01) 120 g 2026-09-04 No No Current