Home NDC 81943-203 X-TERIL
Product NDC 81943-203
11-digit product format 819430203
Labeler code 81943
Product ID 81943-203_440b7c7b-d81f-6284-e063-6394a90a5e1c
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler Aqua Medica, S.A. de C.V.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-03-30
Substance ALCOHOL
Active strength 75 L/100L
NDC exclude flag No
Listing certified through 2026-12-31
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 X-TERIL
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 75 L/100L
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 81943-203-01 X-TERIL 1000 mL in 1 BOTTLE GEL 1000 6 81943-203-02 X-TERIL 3785 mL in 1 BOTTLE GEL 3785 6 81943-203-03 X-TERIL 20 L in 1 DRUM GEL 20 2
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 · 3 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81943-203-01 81943020301 1000 mL in 1 BOTTLE (81943-203-01) 1000 ml 2020-03-30 No No Current 81943-203-02 81943020302 3785 mL in 1 BOTTLE (81943-203-02) 3785 ml 2020-03-30 No No Current 81943-203-03 81943020303 20 L in 1 DRUM (81943-203-03) 20 l 2020-03-30 No No Current