FDA.reportPublic FDA data

NATRUM CARBONICUM

Product NDC
62106-5189
11-digit product format
621065189
Labeler code
62106
Product ID
62106-5189_ececf4c5-69e5-c2fd-e053-2995a90ab78e
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium carbonate
Dosage form
GRANULE
Route
ORAL
Labeler
Seroyal USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-12
Marketing end
0000-00-00
Substance
SODIUM CARBONATE
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct62106-5189DDiscontinued by firm2026-07-31
excluded packagepackage62106-518962106-5189-4DDiscontinued by firm2026-07-31

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM CARBONATEACTIVE INGREDIENT45P3261C7TNATRUM CARBONICUM (SODIUM CARBONATE) GRANULE [SEROYAL USA]1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7DNATRUM CARBONICUM (SODIUM CARBONATE) GRANULE [SEROYAL USA]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GNATRUM CARBONICUM (SODIUM CARBONATE) GRANULE [SEROYAL USA]1
SUCROSEINACTIVE INGREDIENTC151H8M554NATRUM CARBONICUM (SODIUM CARBONATE) GRANULE [SEROYAL USA]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62106-5189-46210651890410 TUBE in 1 CARTON (62106-5189-4) > 140 GRANULE in 1 TUBE10 tube2015-06-120000-00-00NoNoCurrent