Universal 70% Rubbing Alcohol

Product NDC
52000-411
11-digit product format
520000411
Labeler code
52000
Product ID
52000-411_ef7afdb7-ad95-436c-82e7-19a7adfabc1d
Type
HUMAN OTC DRUG
Nonproprietary name
Isopropyl alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
Universal Distribution Center LLC
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-07-01
Substance
ISOPROPYL ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Universal 70% Rubbing Alcohol
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ISOPROPYL ALCOHOL70 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiND2M416302
Rxcui808520

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-411-32Universal 70% Rubbing Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-411UNIVERSAL 70% RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]2Current NDC, 1 package rows20241212_d8b9b0e7-2cb8-4fc5-af55-790e64d6cfe8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
808520isopropyl alcohol 70 % Topical SolutionPSNd8b9b0e7-2cb8-4fc5-af55-790e64d6cfe82
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCDd8b9b0e7-2cb8-4fc5-af55-790e64d6cfe82
808520isopropyl alcohol 70 % Topical SolutionSYd8b9b0e7-2cb8-4fc5-af55-790e64d6cfe82

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
52000-411-3252000041132946 mL in 1 BOTTLE, PLASTIC (52000-411-32) 946 ml2023-07-01NoNoCurrent