Connection

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: Connection
Generic name: ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA, GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 214eb19a-e7a2-421c-9f34-724ce430185c
SPL ID: f6beea73-ec85-4b1b-8dcb-88ff69530137
Version: 2
Effective date: 2026-04-10
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:23

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Connection	openfda.brand_name
generic name		ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA, GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2356-1	openfda.package_ndc
ndc	product	43742-2356	openfda.product_ndc
ndc11	package	43742235601	derived:openfda.package_ndc
spl id		f6beea73-ec85-4b1b-8dcb-88ff69530137	id
spl set id		214eb19a-e7a2-421c-9f34-724ce430185c	set_id
unii		C151H8M554	openfda.unii
unii		51FI676N6F	openfda.unii
unii		7YNJ3PO35Z	openfda.unii
unii		C8CV8867O8	openfda.unii
unii		608DGJ6815	openfda.unii
unii		1NT28V9397	openfda.unii
unii		G39P120JQT	openfda.unii
unii		1JQS135EYN	openfda.unii
unii		4VB4Y46AHD	openfda.unii
unii		N20HL7Q941	openfda.unii
unii		RHH784E0K6	openfda.unii
unii		3A3U0GI71G	openfda.unii
unii		G6W4F0V8Z3	openfda.unii
unii		45P3261C7T	openfda.unii
unii		Y0F0BU8RDU	openfda.unii
unii		00072J7XWS	openfda.unii
unii		2BMD2GNA4V	openfda.unii
unii		7FT6QUT299	openfda.unii
unii		1XCH439UQR	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, 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.