Erbium Sulphuricum

Product NDC
37662-2923
Requested package NDC
37662-2923-2
11-digit product format
376622923
Labeler code
37662
Product ID
37662-2923_f8a19f14-edd5-d02c-e053-6394a90afc99
Type
HUMAN OTC DRUG
Nonproprietary name
Erbium Sulphuricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-04-05
Substance
ERBIUM SULFATE OCTAHYDRATE
Active strength
500 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Erbium Sulphuricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ERBIUM SULFATE OCTAHYDRATE500 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
76R3969825Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f8a19f14-edd4-d02c-e053-6394a90afc99Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2923-1Erbium Sulphuricum200 in 1 VIAL, GLASSPELLET2001
37662-2923-2Erbium Sulphuricum500 in 1 VIAL, GLASSPELLET5001
37662-2923-3Erbium Sulphuricum3000 in 1 BOTTLE, GLASSPELLET30001
37662-2923-4Erbium Sulphuricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2923ERBIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230408_f8a19f14-edd4-d02c-e053-6394a90afc99.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
Erbium SulphuricumERBIUM SULPHURICUMHahnemann Laboratories, INC.f8a19f14-edd4-d02c-e053-6394a90afc992023-04-05Exact identifier
ndc (package): 37662-2923-2
ndc (product): 37662-2923
ndc11 (package): 37662292302

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2923-237662292302500 PELLET in 1 VIAL, GLASS (37662-2923-2) 500 pellet2023-04-05NoNoCurrent