Metals

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: Metals
Generic name: ALUMINA, AURUM METALLICUM, CARBO VEGETABILIS, CAUSTICUM, CYSTEINUM, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, NITRICUM ACIDUM, NUX VOMICA, PHYTOLACCA DECANDRA, PLATINUM METALLICUM, STANNUM METALLICUM, STILLINGIA SYLVATICA, TELLURIUM METALLICUM, X-RAY
Manufacturer: Liddell Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: daa89e0d-1dd8-45eb-9f9b-0029fdcfecee
SPL ID: 59b8ee19-571c-4f9c-9ff8-15ef16939cb6
Version: 3
Effective date: 2024-07-01
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:25

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Metals	openfda.brand_name
generic name		ALUMINA, AURUM METALLICUM, CARBO VEGETABILIS, CAUSTICUM, CYSTEINUM, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, NITRICUM ACIDUM, NUX VOMICA, PHYTOLACCA DECANDRA, PLATINUM METALLICUM, STANNUM METALLICUM, STILLINGIA SYLVATICA, TELLURIUM METALLICUM, X-RAY	openfda.generic_name
manufacturer name		Liddell Laboratories, Inc.	openfda.manufacturer_name
ndc	package	50845-0249-1	openfda.package_ndc
ndc	package	50845-0249-2	openfda.package_ndc
ndc	product	50845-0249	openfda.product_ndc
ndc11	package	50845024902	derived:openfda.package_ndc
ndc11	package	50845024901	derived:openfda.package_ndc
spl id		59b8ee19-571c-4f9c-9ff8-15ef16939cb6	id
spl set id		daa89e0d-1dd8-45eb-9f9b-0029fdcfecee	set_id
unii		2P3VWU3H10	openfda.unii
unii		387GMG9FH5	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		LMI26O6933	openfda.unii
unii		269XH13919	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		K848JZ4886	openfda.unii
unii		6PRJ93602P	openfda.unii
unii		QBR70R4FBK	openfda.unii
unii		NQA0O090ZJ	openfda.unii
unii		6EC706HI7F	openfda.unii
unii		1MBW07J51Q	openfda.unii
unii		49DFR088MY	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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a doctor before using product. Store at room temperature. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Reported adverse events (FAERS/openFDA)#

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