Immunogesic

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: Immunogesic
Generic name: ARNICA MONTANA, APIS MELLIFICA, BENZOICUM ACIDUM, CARTILAGO SUIS, LEDUM PALUSTRE, PANTOTHENIC ACID, RUTA GRAVEOLENS, RHODODENDRON CHRYSANTHUM, CAUSTICUM, FORMICA RUFA, SEPIA, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CALCAREA PHOSPHORICA, COLCHICUM AUTUMNALE, PHYTOLACCA DECANDRA, RADIUM BROMATUM, RHUS VENENATA, THUJA OCCIDENTALIS, LAC CANINUM
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a7363a92-bcef-450e-9168-39f51a57cf3e
SPL ID: f020d0ad-bbbc-4ec5-85d3-af9dad5787a4
Version: 3
Effective date: 2024-03-07
Source export date: 2026-11-06
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/5781d2d281f00c57d2634422e88d204f4ab5cf8444979f7006f538b3a4f26d3b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:35:02

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Immunogesic	openfda.brand_name
generic name		ARNICA MONTANA, APIS MELLIFICA, BENZOICUM ACIDUM, CARTILAGO SUIS, LEDUM PALUSTRE, PANTOTHENIC ACID, RUTA GRAVEOLENS, RHODODENDRON CHRYSANTHUM, CAUSTICUM, FORMICA RUFA, SEPIA, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CALCAREA PHOSPHORICA, COLCHICUM AUTUMNALE, PHYTOLACCA DECANDRA, RADIUM BROMATUM, RHUS VENENATA, THUJA OCCIDENTALIS, LAC CANINUM	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1971-1	openfda.package_ndc
ndc	product	43742-1971	openfda.product_ndc
ndc11	package	43742197101	derived:openfda.package_ndc
spl id		f020d0ad-bbbc-4ec5-85d3-af9dad5787a4	id
spl set id		a7363a92-bcef-450e-9168-39f51a57cf3e	set_id
unii		877L01IZ0P	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		19F5HK2737	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		993QHL78E6	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		Y3VW699H96	openfda.unii
unii		1NT28V9397	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		N94C2U587S	openfda.unii
unii		G39P120JQT	openfda.unii
unii		73Y7P0K73Y	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		55H0W83JO5	openfda.unii
unii		R74O7T8569	openfda.unii
unii		73ECW5WG2F	openfda.unii
unii		IV92NQJ73U	openfda.unii
unii		7S82P3R43Z	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 breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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