FDA.reportPublic FDA data

Ammonium Bromatum

Manufacturer
Hahnemann Laboratories, Inc.
Effective date
2020-09-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:14:43

Label at a glance#

ProductAmmonium Bromatum
Active ingredientAMMONIUM BROMIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonium Bromatum 500C 1gAmmonium Bromatum 500C 1gAmmonium Bromatum 500C 5gAmmonium Bromatum 500C 5gAmmonium Bromatum 500C 30gAmmonium Bromatum 500C 30gAmmonium Bromatum 500C 100gAmmonium Bromatum 500C 100g

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63545-91663545-916-01, 63545-916-02, 63545-916-03, 63545-916-04

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
NameUNIIKind
SUCROSEC151H8M554IACT
AMMONIUM BROMIDER0JB3224WSACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b016c4da-f13e-7e35-e053-2a95a90a395cafef0b8e-28b3-bd45-e053-2a95a90a86e52020-09-24Exact identifier
spl set id: afef0b8e-28b3-bd45-e053-2a95a90a86e5

Reported adverse events (FAERS/openFDA)#

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