Erbium sulphuricum

Manufacturer: Hahnemann Laboratories, Inc.
Effective date: 2022-07-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:17:53

Label at a glance#

ProductErbium sulphuricum

Active ingredientERBIUM SULFATE OCTAHYDRATE

Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-15.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63545-699-01	2025-01-30	C162847	48780-1	9d75b9d0-e644-f424-e053-dadaa90a57ce	70bc64ea-6e26-77e7-e053-2991aa0a449d
63545-699-01	2022-07-27	C162847	48780-1	9d75b9d0-e644-f424-e053-dadaa90a57ce	70bc64ea-6e26-77e7-e053-2991aa0a449d
63545-699-01	2020-01-31	C162847	48780-1	9d75b9d0-e644-f424-e053-dadaa90a57ce	70bc64ea-6e26-77e7-e053-2991aa0a449d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63545-699-01	Erbium sulphuricum	730 [hp_M] in 1 VIAL, GLASS	PELLET	730		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63545-699	ERBIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.]	2	Legacy NDC, 1 package rows	20220729_70bc64ea-6e26-77e7-e053-2991aa0a449d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Erbium sulphuricum
ERBIUM SULFATE OCTAHYDRATE
ERBIUM
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63545-699	63545-699-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ERBIUM SULFATE OCTAHYDRATE	76R3969825	ACTIB
SUCROSE	C151H8M554	IACT

Source Document#

Source XML

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
e4cf721c-f249-1e51-e053-2a95a90ab668			70bc64ea-6e26-77e7-e053-2991aa0a449d	2022-07-27		Exact identifier spl id: e4cf721c-f249-1e51-e053-2a95a90ab668 spl set id: 70bc64ea-6e26-77e7-e053-2991aa0a449d

Reported adverse events (FAERS/openFDA)#

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