Home NDC 83986-982 Ethyl alcohol 62%
Product NDC 83986-982
11-digit product format 839860982
Labeler code 83986
Product ID 83986-982_59cea08d-299b-2f50-e063-6394a90a6e14
Type HUMAN OTC DRUG
Nonproprietary name Ethyl alcohol 62%
Dosage form LIQUID
Route TOPICAL
Labeler UpLift Brands, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-24
Substance ALCOHOL
Active strength 62 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 Ethyl alcohol 62%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 247835 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 83986-982-16 83986098216 59 mL in 1 BOTTLE, PLASTIC (83986-982-16) 59 ml 2026-08-24 No No Current