Home NDC 57337-104-01 Witch Hazel Pore Clarifying Toner
Product NDC 57337-104
Requested package NDC 57337-104-01
11-digit product format 573370104
Labeler code 57337
Product ID 57337-104_2e00e61d-042b-1f00-e063-6294a90aff43
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid 2%
Dosage form GEL
Route TOPICAL
Labeler Ningbo Rejoice International
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-12-11
Substance SALICYLIC ACID
Active strength 20 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 57337-104 57337-104-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 57337-104 57337-104-01 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 57337-104 57337-104-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 Witch Hazel Pore Clarifying Toner
Brand name suffix 8 oz
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57337-104-01 Witch Hazel Pore Clarifying Toner8 oz 237 mL in 1 BOTTLE GEL 237 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57337-104 WITCH HAZEL PORE CLARIFYING TONER 8 OZ (SALICYLIC ACID 2%) GEL [NINGBO REJOICE INTERNATIONAL] 2 Current NDC, Legacy NDC, 1 package rows 20250215_99748785-8321-7bbf-e053-2a95a90a16c9.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 42 of 54 · 1,079 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 57337-104-01 57337010401 237 mL in 1 BOTTLE (57337-104-01) 237 ml 2019-12-11 0000-00-00 No No Current