Home NDC 57337-062-01 XtraCare Wet Wipes
Product NDC 57337-062
Requested package NDC 57337-062-01
11-digit product format 573370062
Labeler code 57337
Product ID 57337-062_2decd513-1fc5-1793-e063-6294a90a18bf
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride
Dosage form SWAB
Route TOPICAL
Labeler Rejoice International
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-03-13
Substance BENZETHONIUM CHLORIDE
Active strength 3 mg/100mg
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 57337-062 57337-062-01 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 57337-062 57337-062-01 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 57337-062 57337-062-01 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 XtraCare Wet Wipes
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE 3 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043348 Internal RxNorm 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 57337-062-01 XtraCare Wet Wipes 100 mg in 1 APPLICATOR SWAB 100 3 57337-062-01 XtraCare Wet Wipes 18 in 1 PACKAGE SWAB 18 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57337-062 XTRACARE WET WIPES (BENZETHONIUM CHLORIDE) SWAB [REJOICE INTERNATIONAL] 3 Current NDC, Legacy NDC, 2 package rows 20250214_3741acc3-c590-4bf1-8c83-4f812e2c7adc.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 100 of 114 · 2,277 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57337-062-01 57337006201 18 APPLICATOR in 1 PACKAGE (57337-062-01) / 100 mg in 1 APPLICATOR 18 applicator 2014-03-13 0000-00-00 No No Current