FDA.reportPublic FDA data

Aurum muriaticum natronatum

Product NDC
0220-0649
11-digit product format
002200649
Labeler code
0220
Product ID
0220-0649_09acadb7-c0a1-d753-e063-6294a90af9a9
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
9 [hp_C]/9[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 TETRACHLOROAURATE9 [hp_C]/9[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
84005bc3-6562-5b9d-e053-2991aa0aef14Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0649-412023-11-08C16284748780-1f386c649-c530-0266-e053-dadaa90a7c1aAurum muriaticum natronatum 9C
0220-0649-412023-01-30C16284748780-1f386c649-c530-0266-e053-dadaa90a7c1aAurum muriaticum natronatum 9C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0649-41Aurum muriaticum natronatum9 [hp_C] in 1 TUBEPELLET92

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0649AURUM MURIATICUM NATRONATUM (SODIUM TETRACHLOROAURATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231109_84005bc3-6562-5b9d-e053-2991aa0aef14.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 TETRACHLOROAURATEBoiron84005bc3-6562-5b9d-e053-2991aa0aef142023-11-08Exact identifier
ndc (product): 0220-0649

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0649-41002200649419 [hp_C] in 1 TUBE (0220-0649-41) 1983-03-030000-00-00NoNoCurrent