Ethyl Alcohol

Product NDC
83986-969
11-digit product format
839860969
Labeler code
83986
Product ID
83986-969_4f58eda2-ba65-b0b9-e063-6394a90a81c2
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
UpLift Brands, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-12-06
Substance
ALCOHOL
Active strength
62 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ethyl Alcohol
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui581660

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-969-16Ethyl Alcohol59 mL in 1 BOTTLE, PLASTICGEL595
83986-969-34Ethyl Alcohol236 mL in 1 BOTTLE, PLASTICGEL2365
83986-969-86Ethyl Alcohol1000 mL in 1 BOTTLE, PLASTICGEL10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83986-969ETHYL ALCOHOL GEL [UPLIFT BRANDS, LLC]1Current NDC, 3 package rows20241208_289d6e34-4d71-b24e-e063-6394a90ac26d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581660ethanol 62 % Topical GelPSN289d6e34-4d71-b24e-e063-6394a90ac26d5
581660ethanol 0.62 ML/ML Topical GelSCD289d6e34-4d71-b24e-e063-6394a90ac26d5
581660ethanol 62 % Topical GelSY289d6e34-4d71-b24e-e063-6394a90ac26d5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83986-969-168398609691659 mL in 1 BOTTLE, PLASTIC59 mlHistorical
83986-969-3483986096934236 mL in 1 BOTTLE, PLASTIC (83986-969-34) 236 ml2024-12-06NoNoCurrent
83986-969-86839860969861000 mL in 1 BOTTLE, PLASTIC (83986-969-86) 1000 ml2025-06-20NoNoCurrent