Home NDC 84167-837 Clopoat CLOPOAT ACNE-CLEARING SPOT
Product NDC 84167-837
11-digit product format 841670837
Labeler code 84167
Product ID 84167-837_53cd1d6b-d44d-2508-e063-6294a90a96c6
Type HUMAN OTC DRUG
Nonproprietary name COLLOIDAL SULFUR
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Meixi Biotechnology Co., Ltd.
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-15
Substance SULFUR
Active strength 3 g/1
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 Clopoat CLOPOAT ACNE-CLEARING SPOT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 3 g/1
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 199632 Internal RxNorm 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 42 of 55 · 1,088 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84167-837-17 84167083717 1 BAG in 1 BOX (84167-837-17) / 1 CREAM in 1 BAG 1 bag 2026-06-15 No No Current