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

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 Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M

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