Dri-Ear

Product NDC
12258-153
11-digit product format
122580153
Labeler code
12258
Product ID
12258-153_47e0bf6b-1109-c48a-e063-6394a90adef3
Type
HUMAN OTC DRUG
Nonproprietary name
Dri-Ear
Dosage form
SUSPENSION/ DROPS
Route
AURICULAR (OTIC)
Labeler
S.S.S. Company
Application
M014
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-04-30
Substance
ISOPROPYL ALCOHOL
Active strength
950 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
Dri-Ear
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ISOPROPYL ALCOHOL950 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiND2M416302

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12258-153-01Dri-Ear30 mL in 1 BOTTLESUSPENSION/ DROPS302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12258-153DRI-EAR SUSPENSION/ DROPS [S.S.S. COMPANY]1Current NDC, 1 package rows20240430_12f07636-bb60-5fd4-e063-6294a90a39a8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
12258-153-011225801530130 mL in 1 BOTTLE (12258-153-01) 30 ml2024-04-30NoNoHistorical