Home NDC 52915-075 EUCALYPTUS EASE HAND SANITIZER
Product NDC 52915-075
11-digit product format 529150075
Labeler code 52915
Product ID 52915-075_8f66cb5a-4877-4d85-8cc6-560590415369
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form SPRAY
Route TOPICAL
Labeler ORGANIC & SUSTAINABLE BEAUTY
Application M004
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-01
Substance ALCOHOL
Active strength 62 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 EUCALYPTUS EASE HAND SANITIZER
Listing expiration 2026-12-31 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 1020364 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52915-075-19 EUCALYPTUS EASE HAND SANITIZER 562 mL in 1 BOTTLE, SPRAY SPRAY 562 2 52915-075-20 EUCALYPTUS EASE HAND SANITIZER 59 mL in 1 BOTTLE, SPRAY SPRAY 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52915-075 EUCALYPTUS EASE HAND SANITIZER (ALCOHOL) SPRAY [ORGANIC & SUSTAINABLE BEAUTY] 2 Current NDC, Legacy NDC, 2 package rows 20241108_09d77591-9472-4771-9090-3390bddf788a.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 22 of 22 · 424 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Family Wellness Antiseptic and Pain Relief BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE FRONT PHARMACEUTICAL PLC cb7fdcde-2bd8-4834-ba4e-4d6fd1512599 2023-10-26 Warnings Exact identifier application number: M004 GENUINE FIRST AID Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. 23abfe12-5b50-4b49-878e-4fcdb6c341fd 2023-10-19 Warnings Exact identifier application number: M004 EVERLIT CARE Triple Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. f4921508-c32f-426f-a2f0-16c3acbd4713 2023-10-14 Warnings Exact identifier application number: M004 Cuadriderma BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE ProMex LLC 4fa99b96-ab4b-4523-82bc-343dbaf39fb6 2022-01-25 Warnings Exact identifier application number: M004
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 52915-075-19 52915007519 562 mL in 1 BOTTLE, SPRAY (52915-075-19) 562 ml 2020-02-01 0000-00-00 No No Current 52915-075-20 52915007520 59 mL in 1 BOTTLE, SPRAY (52915-075-20) 59 ml 2020-02-01 0000-00-00 No No Current