FDA.reportPublic FDA data

NATRIUM PHOSPHORICUM 6X

Product NDC
62106-1059
11-digit product format
621061059
Labeler code
62106
Product ID
62106-1059_c71d7cd0-09ad-bb0b-e053-2995a90ac703
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Phosphate
Dosage form
TABLET
Route
SUBLINGUAL
Labeler
Seroyal USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-10-23
Substance
SODIUM PHOSPHATE
Active strength
6 [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
NATRIUM PHOSPHORICUM 6X
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM PHOSPHATE6 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
SE337SVY37Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
22cc1c1e-626f-4a15-e054-00144ff88e88Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1059-2NATRIUM PHOSPHORICUM 6X100 in 1 BOTTLE, GLASSTABLET1005
62106-1059-2NATRIUM PHOSPHORICUM 6X1 in 1 CARTONTABLET15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM PHOSPHATEACTIVE INGREDIENTSE337SVY37NATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1
PHOSPHATE IONACTIVE MOIETYNK08V8K8HRNATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48NATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XNATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30NATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1
XYLITOLINACTIVE INGREDIENTVCQ006KQ1ENATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1059NATRIUM PHOSPHORICUM 6X (SODIUM PHOSPHATE) TABLET [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20210715_22cc1c1e-626f-4a15-e054-00144ff88e88.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NATRIUM PHOSPHORICUM 6XSODIUM PHOSPHATESeroyal USA22cc1c1e-626f-4a15-e054-00144ff88e882021-07-14WarningsExact identifier
ndc (product): 62106-1059

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
62106-1059-2621061059021 BOTTLE, GLASS in 1 CARTON (62106-1059-2) / 100 TABLET in 1 BOTTLE, GLASS2015-10-230000-00-00NoNoCurrent