FDA.reportPublic FDA data

Aurum metallicum

Product NDC
0220-0671
11-digit product format
002200671
Labeler code
0220
Product ID
0220-0671_f527fe86-7d8d-5cbe-e053-2995a90a4b35
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
10 [hp_M]/10[hp_M]
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
GOLD10 [hp_M]/10[hp_M]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii79Y1949PYO

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0671-412023-02-20C16284748780-1f386c649-d942-0266-e053-dadaa90a7c1aAurum metallicum 10M
0220-0671-412023-01-30C16284748780-1f386c649-d942-0266-e053-dadaa90a7c1aAurum metallicum 10M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0671-41Aurum metallicum10 [hp_M] in 1 TUBEPELLET102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0671AURUM METALLICUM (GOLD) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230221_84f10008-5c27-43b4-e053-2a91aa0a64b9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0671-410022006714110 [hp_M] in 1 TUBE (0220-0671-41) 1983-03-030000-00-00NoNoCurrent