DermaMed

Product NDC
61924-214
11-digit product format
619240214
Labeler code
61924
Product ID
61924-214_9c59a3bf-a4d4-2fdd-e053-2a95a90a1c67
Type
HUMAN OTC DRUG
Nonproprietary name
Skin Protectant
Dosage form
OINTMENT
Route
TOPICAL
Labeler
DermaRite Industries, LLC
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-10-18
Marketing end
0000-00-00
Substance
ALUMINUM HYDROXIDE
Active strength
2 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61924-214-042024-12-06C16284748780-1d6a99b39-8624-a426-e053-dadaa90af4c2DermaMed
61924-214-042022-01-28C16284748780-1d6a99b39-8624-a426-e053-dadaa90af4c2DermaMed

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61924-214-04DermaMed106 g in 1 TUBEOINTMENT1063

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61924-214-04GM - Gram61924-2147a829a84-3808-4cd3-a658-67c090c6769a12017-11-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61924-214DERMAMED (SKIN PROTECTANT) OINTMENT [DERMARITE INDUSTRIES, LLC]3Legacy NDC, 1 package rows20241208_5bd4173d-8794-3d28-e053-2991aa0a06a9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61924-214-0461924021404106 g in 1 TUBE (61924-214-04) 106 g2016-10-180000-00-00NoNoCurrent