Home NDC 53942-810 70%
Product NDC 53942-810
11-digit product format 539420810
Labeler code 53942
Product ID 53942-810_49f111fb-cea3-ca3f-e063-6294a90ab3b1
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Demoulas Super Markets, Inc
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2003-11-24
Substance ISOPROPYL ALCOHOL
Active strength 70 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, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…
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 70%
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 808520 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 53942-810-43 70% 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 7 53942-810-45 70% 946 mL in 1 BOTTLE, PLASTIC LIQUID 946 7 53942-810-72 70% 295 mL in 1 BOTTLE, SPRAY LIQUID 295 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53942-810 70% (ISOPROPYL ALCOHOL) LIQUID [DEMOULAS SUPER MARKETS, INC] 6 Current NDC, Legacy NDC, 3 package rows 20250309_7cbd8ef5-9744-49ad-9640-d4c2b1ae8203.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 53942-810-43 53942081043 473 mL in 1 BOTTLE, PLASTIC (53942-810-43) 473 ml 2003-11-24 0000-00-00 No No Current 53942-810-45 53942081045 946 mL in 1 BOTTLE, PLASTIC (53942-810-45) 946 ml 2003-11-24 0000-00-00 No No Current 53942-810-72 53942081072 295 mL in 1 BOTTLE, SPRAY (53942-810-72) 295 ml 2003-11-24 0000-00-00 No No Current