Avagard D

Product NDC
48878-0231
11-digit product format
488780231
Labeler code
48878
Product ID
48878-0231_5e2221bd-9805-4950-a952-5f726f8e2dda
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
LOTION
Route
TOPICAL
Labeler
Solventum US LLC
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1999-10-01
Substance
ALCOHOL
Active strength
530.7 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
Avagard D
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL530.7 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48878-0231-7Avagard D12 in 1 CASELOTION129
48878-0231-7Avagard D500 mL in 1 BOTTLELOTION5009

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48878-0231AVAGARD D (ALCOHOL) LOTION [SOLVENTUM US OPCO LLC]8Current NDC, Legacy NDC, 2 package rows20240329_00c56d8d-02e6-4839-86cc-00767428d5e9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48878-0231-74887802310712 BOTTLE in 1 CASE (48878-0231-7) / 500 mL in 1 BOTTLE12 bottle2011-04-280000-00-00NoNoCurrent