FDA.reportPublic FDA data

Natrum phosphoricum

Product NDC
0220-3608
Requested package NDC
0220-3608-41
11-digit product format
002203608
Labeler code
0220
Product ID
0220-3608_0a1fbdfd-54f2-cbfd-e063-6394a90a2db8
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Natrum phosphoricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
70WT22SF4BInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
86472dc7-5d6a-c3bc-e053-2a91aa0a0e63Available 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3608-412023-11-14C16284748780-1f386c649-d54c-0266-e053-dadaa90a7c1aNatrum phosphoricum 30C
0220-3608-412023-01-30C16284748780-1f386c649-d54c-0266-e053-dadaa90a7c1aNatrum phosphoricum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3608-41Natrum phosphoricum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3608NATRUM PHOSPHORICUM (SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231115_86472dc7-5d6a-c3bc-e053-2a91aa0a0e63.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
Natrum phosphoricumSODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATEBoiron86472dc7-5d6a-c3bc-e053-2a91aa0a0e632023-11-14Exact identifier
ndc (package): 0220-3608-41
ndc (product): 0220-3608
ndc11 (package): 00220360841

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3608-410022036084130 [hp_C] in 1 TUBE (0220-3608-41) 1983-03-030000-00-00NoNoCurrent