Home NDC 52410-1050 NOVITA ISOPROPYL ALCOHOL 50%
Product NDC 52410-1050
11-digit product format 524101050
Labeler code 52410
Product ID 52410-1050_4d3bfa8e-2f33-65fe-e063-6394a90a448a
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Shield Line LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-08-24
Substance ISOPROPYL ALCOHOL
Active strength 50 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 52410-1050-4 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 52410-1050-4 f5e01cc5f278…a2eaf40c39c3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 52410-1050-4 1332a3947898…d4bfe170f9cd…
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 NOVITA ISOPROPYL ALCOHOL 50%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 50 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 616456 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 52410-1050-4 NOVITA ISOPROPYL ALCOHOL 50% 355 mL in 1 BOTTLE, PLASTIC LIQUID 355 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52410-1050 NOVITA ISOPROPYL ALCOHOL 50% (ISOPROPYL ALCOHOL) LIQUID [SHIELD LINE LLC] 3 Current NDC, Legacy NDC, 1 package rows 20240418_3ad79e91-377d-6587-e054-00144ff8d46c.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 52410-1050-4 52410105004 355 mL in 1 BOTTLE, PLASTIC (52410-1050-4) 355 ml 2016-08-24 0000-00-00 No No Current