Homeoplex D

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: Homeoplex D
Generic name: GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,
Manufacturer: Supplement Clinic, LLC.
Product type: HUMAN OTC DRUG
SPL set ID: cd6b48ab-3566-484d-8deb-15ef6f8e7e8f
SPL ID: b4f1a644-707b-4b5f-b9ae-355e323183b8
Version: 1
Effective date: 2017-11-01
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:38

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 2 · 42 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Homeoplex D	openfda.brand_name
generic name		GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,	openfda.generic_name
manufacturer name		Supplement Clinic, LLC.	openfda.manufacturer_name
ndc	package	71781-0003-1	openfda.package_ndc
ndc	product	71781-0003	openfda.product_ndc
ndc11	package	71781000301	derived:openfda.package_ndc
spl id		b4f1a644-707b-4b5f-b9ae-355e323183b8	id
spl set id		cd6b48ab-3566-484d-8deb-15ef6f8e7e8f	set_id
unii		27YLU75U4W	openfda.unii
unii		6RV024OAUQ	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		VCQ006KQ1E	openfda.unii
unii		269XH13919	openfda.unii
unii		8CRQ2TH63M	openfda.unii
unii		R57ZHV85D4	openfda.unii
unii		4T6H12BN9U	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		1VPU26JZZ4	openfda.unii
unii		4R7X1O2820	openfda.unii
unii		411VRN1TV4	openfda.unii
unii		O414PZ4LPZ	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		PDC6A3C0OX	openfda.unii
unii		AVT680JB39	openfda.unii
unii		Q40Q9N063P	openfda.unii
unii		39981FM375	openfda.unii
unii		R16CO5Y76E	openfda.unii
unii		3T8H1794QW	openfda.unii
unii		K0U68Q2TXA	openfda.unii
unii		LKG8494WBH	openfda.unii
unii		GN5P7K3T8S	openfda.unii
unii		YUL4LO94HK	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		2DI9HA706A	openfda.unii
unii		3B8D35Y7S4	openfda.unii
unii		2P299V784P	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		G59M7S0WS3	openfda.unii
unii		506T60A25R	openfda.unii
unii		2BMD2GNA4V	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: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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