FDA.reportPublic FDA data

Aurum metallicum

Product NDC
0220-0667
11-digit product format
002200667
Labeler code
0220
Product ID
0220-0667_09ac8fbe-166d-c886-e063-6294a90a6209
Type
HUMAN OTC DRUG
Nonproprietary name
GOLD
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
GOLD
Active strength
15 [hp_C]/15[hp_C]
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Aurum metallicum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GOLD15 [hp_C]/15[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii79Y1949PYO

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0667-412023-11-08C16284748780-1f386c649-b5be-0266-e053-dadaa90a7c1aAurum metallicum 15C
0220-0667-412023-01-30C16284748780-1f386c649-b5be-0266-e053-dadaa90a7c1aAurum metallicum 15C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0667-41Aurum metallicum15 [hp_C] in 1 TUBEPELLET152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0667AURUM METALLICUM (GOLD) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231109_84629c2b-ce31-bf90-e053-2a91aa0a21f7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0667-410022006674115 [hp_C] in 1 TUBE (0220-0667-41) 1983-03-030000-00-00NoNoCurrent