Argentum metallicum

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Argentum metallicum
Generic name: ARGENTUM METALLICUM
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: fb46f80f-a50b-f8d2-e053-6394a90a077d
SPL ID: fb471672-91d5-9aed-e053-6294a90a74d3
Version: 1
Effective date: 2023-05-09
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:24:28

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Argentum metallicum	openfda.brand_name
generic name		ARGENTUM METALLICUM	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-9024-7	openfda.package_ndc
ndc	product	55714-9024	openfda.product_ndc
ndc11	package	55714902407	derived:openfda.package_ndc
spl id		fb471672-91d5-9aed-e053-6294a90a74d3	id
spl set id		fb46f80f-a50b-f8d2-e053-6394a90a077d	set_id
unii		3M4G523W1G	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS SECTION Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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