Alcohol

Product NDC
69790-849
Requested package NDC
69790-849-55
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

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
fdda41fa-d847-4cee-a070-91f0600b0fc8Available on FDA.report

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

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AlcoholALCOHOLUlinefdda41fa-d847-4cee-a070-91f0600b0fc82026-02-17Warnings, Adverse reactionsExact identifier
ndc (package): 69790-849-55
ndc (product): 69790-849
ndc11 (package): 69790084955

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69790-849-55697900849552082 mL in 1 DRUM (69790-849-55) 2082 ml2020-08-140000-00-00NoNoCurrent