FDA.reportPublic FDA data

Aurum muriaticum natronatum

Product NDC
0220-0648
Requested package NDC
0220-0648-41
11-digit product format
002200648
Labeler code
0220
Product ID
0220-0648_09acb03c-1113-b167-e063-6394a90aaee1
Type
HUMAN OTC DRUG
Nonproprietary name
SODIUM TETRACHLOROAURATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
SODIUM TETRACHLOROAURATE
Active strength
4 [hp_C]/4[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
Aurum muriaticum natronatum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM TETRACHLOROAURATE4 [hp_C]/4[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7FT6QUT299Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
84005c8d-3ff5-48bb-e053-2a91aa0ab3b4Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0648-412023-11-08C16284748780-1f386c64a-209d-0266-e053-dadaa90a7c1aAurum muriaticum natronatum 4C
0220-0648-412023-01-30C16284748780-1f386c64a-209d-0266-e053-dadaa90a7c1aAurum muriaticum natronatum 4C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0648-41Aurum muriaticum natronatum4 [hp_C] in 1 TUBEPELLET42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0648AURUM MURIATICUM NATRONATUM (SODIUM TETRACHLOROAURATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231109_84005c8d-3ff5-48bb-e053-2a91aa0ab3b4.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
Aurum muriaticum natronatumSODIUM TETRACHLOROAURATEBoiron84005c8d-3ff5-48bb-e053-2a91aa0ab3b42023-11-08Exact identifier
ndc (package): 0220-0648-41
ndc (product): 0220-0648
ndc11 (package): 00220064841

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0648-41002200648414 [hp_C] in 1 TUBE (0220-0648-41) 1983-03-030000-00-00NoNoCurrent