Alcohol

Product NDC
69790-849
11-digit product format
697900849
Labeler code
69790
Product ID
69790-849_5f61df31-1336-1703-e063-6294a90ac4f2
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage69790-84969790-849-55DDiscontinued by firm2026-11-06
excluded packagepackage69790-84969790-849-68DDiscontinued by firm2026-11-06

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 dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage69790-84969790-849-68DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage69790-84969790-849-68DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…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
Alcohol
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 mg/mL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69790-849-08Alcohol3785 mL in 1 BOTTLE, PLASTICLIQUID37859
69790-849-55Alcohol2082 mL in 1 DRUMLIQUID20829
69790-849-68Alcohol2000 mL in 1 BOTTLE, PLASTICLIQUID20009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69790-849ALCOHOL LIQUID [ULINE]7Current NDC, Legacy NDC, 3 package rows20240929_fdda41fa-d847-4cee-a070-91f0600b0fc8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69790-849-08697900849083785 mL in 1 BOTTLE, PLASTIC (69790-849-08) 3785 ml2019-07-190000-00-00NoNoCurrent
69790-849-55697900849552082 mL in 1 DRUM (69790-849-55) 2082 ml2020-08-140000-00-00NoNoCurrent
69790-849-68697900849682000 mL in 1 BOTTLE, PLASTIC (69790-849-68) 2000 ml2020-07-020000-00-00NoNoCurrent