Aurum metallicum

Product NDC: 0220-0669
11-digit product format: 002200669
Labeler code: 0220
Product ID: 0220-0669_fd668eff-5829-259d-e053-6394a90a1a1e
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: 200 [kp_C]/200[kp_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
Ingredient	Strength
GOLD	200 [kp_C]/200[kp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
79Y1949PYO	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
84f0ac34-f7e2-16e9-e053-2991aa0a6756	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0220-0669-41	2023-06-05	C162847	48780-1	f386c649-b31d-0266-e053-dadaa90a7c1a	Aurum metallicum 200CK
0220-0669-41	2023-01-30	C162847	48780-1	f386c649-b31d-0266-e053-dadaa90a7c1a	Aurum metallicum 200CK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0220-0669-41	Aurum metallicum	200 [kp_C] in 1 TUBE	PELLET	200		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0220-0669	AURUM METALLICUM (GOLD) PELLET [BOIRON]	2	Current NDC, Legacy NDC, 1 package rows	20230607_84f0ac34-f7e2-16e9-e053-2991aa0a6756.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aurum metallicum	GOLD	Boiron	84f0ac34-f7e2-16e9-e053-2991aa0a6756	2023-06-05		Exact identifier ndc (product): 0220-0669

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
79Y1949PYO	GOLD	7440-57-5	GOLD

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0220-0669-41	00220066941	200 [kp_C] in 1 TUBE (0220-0669-41)	1983-03-03	0000-00-00	No	No	Current