Home NDC 47593-658-41 XHC-075
Product NDC 47593-658
Requested package NDC 47593-658-41
11-digit product format 475930658
Labeler code 47593
Product ID 47593-658_4b521555-ef7e-418b-af98-977af638f783
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form SOLUTION
Route TOPICAL
Labeler Ecolab Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-07
Substance ALCOHOL
Active strength 68.4 mL/100mL
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 XHC-075
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 68.4 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 47593-658-41 XHC-075 750 mL in 1 BOTTLE, PLASTIC SOLUTION 750 1 47593-658-70 XHC-075 1200 mL in 1 BOTTLE, PLASTIC SOLUTION 1200 1
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 47593-658-41 47593065841 750 mL in 1 BOTTLE, PLASTIC (47593-658-41) 750 ml 2026-05-07 No No Current