Home FDA labels 446da5cc-e452-4416-a9c4-0788ddc3106b Chronagesic 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 Chronagesic
Generic name ARNICA MONTANA, CINNAMOMUM, DULCAMARA, FUNICULUS UMBILICALIS SUIS, NADIDUM, NATRUM OXALACETICUM, PANTOTHENIC ACID, PLACENTA TOTALIS SUIS, SANGUINARIA CANADENSIS, SULPHUR, PIPER NIGRUM, ALPHA-LIPOICUM ACIDUM, CARTILAGO SUIS, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE, THUJA OCCIDENTALIS, APIOLUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN PRESCRIPTION DRUG
SPL set ID 66e351ed-d359-4367-a950-fc57b37489ab
SPL ID 446da5cc-e452-4416-a9c4-0788ddc3106b
Version 5
Effective date 2024-09-11
Source export date 2026-10-27
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:59:53 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Chronagesic openfda.brand_name generic name ARNICA MONTANA, CINNAMOMUM, DULCAMARA, FUNICULUS UMBILICALIS SUIS, NADIDUM, NATRUM OXALACETICUM, PANTOTHENIC ACID, PLACENTA TOTALIS SUIS, SANGUINARIA CANADENSIS, SULPHUR, PIPER NIGRUM, ALPHA-LIPOICUM ACIDUM, CARTILAGO SUIS, RHUS TOX, SILICEA, SYMPHYTUM OFFICINALE, THUJA OCCIDENTALIS, APIOLUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1665-1 openfda.package_ndc ndc product 43742-1665 openfda.product_ndc ndc11 package 43742166501 derived:openfda.package_ndc spl id 446da5cc-e452-4416-a9c4-0788ddc3106b id spl set id 66e351ed-d359-4367-a950-fc57b37489ab set_id unii 5S29HWU6QB openfda.unii unii 19F5HK2737 openfda.unii unii 6G53L8ESRK openfda.unii unii C8CV8867O8 openfda.unii unii KPS1B1162N openfda.unii unii O80TY208ZW openfda.unii unii 1NT28V9397 openfda.unii unii 73Y7P0K73Y openfda.unii unii ETJ7Z6XBU4 openfda.unii unii M9VVZ08EKQ openfda.unii unii 6IO182RP7A openfda.unii unii 73ECW5WG2F openfda.unii unii 0U46U6E8UK openfda.unii unii 70FD1KFU70 openfda.unii unii QQ67504PXO openfda.unii unii N9288CD508 openfda.unii unii 6CA025Y4FG openfda.unii unii 118OYG6W3H 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: S ealed 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.