Home NDC 57337-036 XtraCare Foaming Facial Cleanser
Product NDC 57337-036
11-digit product format 573370036
Labeler code 57337
Product ID 57337-036_126d79f0-68eb-8a53-e063-6294a90a6fe1
Type HUMAN OTC DRUG
Nonproprietary name Triclosan
Dosage form GEL
Route TOPICAL
Labeler Rejoice International
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-11-26
Substance TRICLOSAN
Active strength 1 mg/237mg
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 XtraCare Foaming Facial Cleanser
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRICLOSAN 1 mg/237mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4NM5039Y5X Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57337-036-01 XtraCare Foaming Facial Cleanser 237 mg in 1 BOTTLE GEL 237 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57337-036 XTRACARE FOAMING FACIAL CLEANSER (TRICLOSAN) GEL [REJOICE INTERNATIONAL] 3 Current NDC, Legacy NDC, 1 package rows 20240229_313fcd4a-8641-417e-bf0b-02359ad815fe.zip
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 52 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57337-036-01 57337003601 237 mg in 1 BOTTLE (57337-036-01) 237 mg 2013-11-26 0000-00-00 No No Current