Home NDC 11673-810-72 70%
Product NDC 11673-810
Requested package NDC 11673-810-72
11-digit product format 116730810
Labeler code 11673
Product ID 11673-810_4b1f8df8-7e36-962f-e063-6394a90a8902
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Target Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 1989-07-15
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 11673-810 11673-810-72 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 11673-810 11673-810-72 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-810-43 70% 473 mL in 1 BOTTLE, PLASTIC LIQUID 473 18 11673-810-45 70% 946 mL in 1 BOTTLE, PLASTIC LIQUID 946 18 11673-810-72 70% 295 mL in 1 BOTTLE, SPRAY LIQUID 295 18
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-810 70% (ISOPROPYL ALCOHOL) LIQUID [TARGET CORP.,] 15 Current NDC, Legacy NDC, 3 package rows 20240726_4db7c9cb-021d-463a-9ff6-91ae42f0311d.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 1 of 1 · 1 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 11673-810-72 11673081072 295 mL in 1 BOTTLE, SPRAY (11673-810-72) 295 ml 1989-07-15 0000-00-00 No No Current