Scholls Wellness Company LLC

Product NDC
73469-7214
11-digit product format
734697214
Labeler code
73469
Product ID
73469-7214_d6569630-4ad5-7173-e053-2995a90a66de
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Sulfide
Dosage form
GEL
Route
TOPICAL
Labeler
Scholls Wellness Company LLC
Application
part358D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-01-01
Marketing end
0000-00-00
Substance
SODIUM SULFIDE
Active strength
1 g/10g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73469-7214-12024-07-30C16284748780-11030e365-2ee7-111a-e063-dadaa90a10e2b7008e97-edb5-3b83-e053-2995a90afde0
73469-7214-12024-01-30C16284748780-11030e365-2ee7-111a-e063-dadaa90a10e2b7008e97-edb5-3b83-e053-2995a90afde0

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73469-7214SCHOLLS WELLNESS COMPANY LLC INGROWN TOENAIL (SODIUM SULFIDE) GEL [SCHOLLS WELLNESS COMPANY LLC]4Legacy NDC20230815_b7008e97-edb5-3b83-e053-2995a90afde0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73469-7214-1734697214011 TUBE in 1 CARTON (73469-7214-1) > 1 g in 1 TUBE1 tube2021-01-010000-00-00NoNoCurrent