Acne Treatment Pads

Product NDC
68062-9004
11-digit product format
680629004
Labeler code
68062
Product ID
68062-9004_50b6e826-3ec8-ee59-e063-6294a90a43eb
Type
HUMAN OTC DRUG
Nonproprietary name
salicylic acid
Dosage form
LOTION
Route
TOPICAL
Labeler
Spa de Soleil
Application
M006
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-09-15
Substance
SALICYLIC ACID
Active strength
1 g/50mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Acne Treatment Pads
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID1 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68062-9004-12023-01-30C16284748780-1f386c649-e5e1-0266-e053-dadaa90a7c1aAcne Treatment Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-9004-1Acne Treatment Pads50 mL in 1 TUBELOTION502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68062-9004ACNE TREATMENT PADS (SALICYLIC ACID) LOTION [SPA DE SOLEIL]1Current NDC, Legacy NDC, 1 package rows20210917_cc0f8f77-1942-22be-e053-2a95a90a3d7f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68062-9004-16806290040150 mL in 1 TUBE (68062-9004-1) 50 ml2021-09-150000-00-00NoNoCurrent