Ammonium Bromtum

Manufacturer: Hahnemann Laboratories, Inc.
Effective date: 2020-09-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:14:34

Label at a glance#

ProductAmmonium Bromtum

Active ingredientAMMONIUM BROMIDE

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonium Bromatum LM1 30g

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Ammonium Bromtum
Ammonium Bromatum
SUCROSE
AMMONIUM BROMIDE
BROMIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63545-918	63545-918-01

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
SUCROSE	C151H8M554	IACT
AMMONIUM BROMIDE	R0JB3224WS	ACTIB

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
b016d7dd-c285-0411-e053-2995a90aceb8			affeb47c-0dfe-7f04-e053-2a95a90a4f1f	2020-09-24		Exact identifier spl set id: affeb47c-0dfe-7f04-e053-2a95a90a4f1f

Reported adverse events (FAERS/openFDA)#

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