Home NDC 87401-000 Youmi Alcohol Prep Pad 70 Isopropyl Alcohol
Product NDC 87401-000
11-digit product format 874010000
Labeler code 87401
Product ID 87401-000_4a6ad128-ef29-63c0-e063-6394a90ab3e3
Type HUMAN OTC DRUG
Nonproprietary name ISOPROPYL ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler PT YOUMI MEDIKA INDUSTRI
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-05
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Youmi Alcohol Prep Pad 70 Isopropyl Alcohol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ND2M416302 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 797544 Internal RxNorm 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 87401-000-00 Youmi Alcohol Prep Pad 70 Isopropyl Alcohol 0.34 mL in 1 POUCH LIQUID 0.34 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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 87401-000-00 87401000000 .34 mL in 1 POUCH (87401-000-00) 2026-02-05 No No Current