Home NDC 69790-849 Alcohol
Product NDC 69790-849
11-digit product format 697900849
Labeler code 69790
Product ID 69790-849_4b09a991-ce1b-ead1-e063-6294a90afce2
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Uline
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-19
Substance ALCOHOL
Active strength 62 mg/mL
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 69790-849 69790-849-68 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 69790-849 69790-849-68 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Additional Listing Data#
Finished product Yes
Brand name base Alcohol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 mg/mL
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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69790-849-08 Alcohol 3785 mL in 1 BOTTLE, PLASTIC LIQUID 3785 9 69790-849-55 Alcohol 2082 mL in 1 DRUM LIQUID 2082 9 69790-849-68 Alcohol 2000 mL in 1 BOTTLE, PLASTIC LIQUID 2000 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69790-849 ALCOHOL LIQUID [ULINE] 7 Current NDC, Legacy NDC, 3 package rows 20240929_fdda41fa-d847-4cee-a070-91f0600b0fc8.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69790-849-08 69790084908 3785 mL in 1 BOTTLE, PLASTIC (69790-849-08) 3785 ml 2019-07-19 0000-00-00 No No Current 69790-849-55 69790084955 2082 mL in 1 DRUM (69790-849-55) 2082 ml 2020-08-14 0000-00-00 No No Current 69790-849-68 69790084968 2000 mL in 1 BOTTLE, PLASTIC (69790-849-68) 2000 ml 2020-07-02 0000-00-00 No No Current