Home NDC 0363-0810 70%
Product NDC 0363-0810
11-digit product format 003630810
Labeler code 0363
Product ID 0363-0810_4a7eb5b3-dae7-4cad-e063-6294a90a1193
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Walgreen Co.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 1989-10-15
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0363-0810 0363-0810-50 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0363-0810 0363-0810-50 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 0363-0810-43 70% 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 17 0363-0810-45 70% 946 mL in 1 BOTTLE, PLASTIC LIQUID 946 17 0363-0810-50 70% 710 mL in 1 BOTTLE, PLASTIC LIQUID 710 17
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0810 70% (ISOPROPYL ALCOHOL) LIQUID [WALGREENS, CO.] 15 Current NDC, Legacy NDC, 3 package rows 20240608_fb918e7a-1fe0-4cfd-8cf0-9d823eb56dcc.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 99 of 114 · 2,270 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 0363-0810-43 00363081043 473 mL in 1 BOTTLE, PLASTIC (0363-0810-43) 473 ml 1989-10-15 0000-00-00 No No Current 0363-0810-45 00363081045 946 mL in 1 BOTTLE, PLASTIC (0363-0810-45) 946 ml 1989-10-15 0000-00-00 No No Current 0363-0810-50 00363081050 710 mL in 1 BOTTLE, PLASTIC (0363-0810-50) 710 ml 1989-10-15 0000-00-00 No No Current