Home NDC 73898-002 Noshinku Eucalyptus Hand Sanitizer
Product NDC 73898-002
11-digit product format 738980002
Labeler code 73898
Product ID 73898-002_187201da-94f8-6de5-e063-6294a90a5c43
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form SOLUTION
Route TOPICAL
Labeler Noshinku
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-07
Substance ALCOHOL
Active strength 70 mL/100mL
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 Noshinku Eucalyptus Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength 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 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 582753 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 73898-002-10 Noshinku Eucalyptus Hand Sanitizer 100 mL in 1 BOTTLE, SPRAY SOLUTION 100 7 73898-002-18 Noshinku Eucalyptus Hand Sanitizer 18 mL in 1 BOTTLE, SPRAY SOLUTION 18 7 73898-002-20 Noshinku Eucalyptus Hand Sanitizer 20 mL in 1 BOTTLE, SPRAY SOLUTION 20 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73898-002 NOSHINKU EUCALYPTUS HAND SANITIZER (ALCOHOL) SOLUTION [NOSHINKU] 7 Current NDC, Legacy NDC, 3 package rows 20240517_9dcb8b51-d1bb-4305-a5ff-8cc8bdcdc4c0.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 9 of 115 · 2,286 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 73898-002-10 73898000210 100 mL in 1 BOTTLE, SPRAY (73898-002-10) 100 ml 2020-12-07 No No Current 73898-002-18 73898000218 18 mL in 1 BOTTLE, SPRAY 18 ml Historical 73898-002-20 73898000220 20 mL in 1 BOTTLE, SPRAY (73898-002-20) 20 ml 2020-12-07 0000-00-00 No No Current