Home FDA labels 5572f8f5-96ae-4a68-82fd-d8f55ae59f77 Dental Pain 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 Dental Pain
Generic name ACETICUM ACIDUM, CALENDULA OFFICINALIS, ZINGIBER OFFICINALE, BRYONIA (ALBA), COFFEA TOSTA, LEDUM PALUSTRE, PHOSPHORUS, PLANTAGO MAJOR, SPIGELIA ANTHELMIA, ARNICA MONTANA, CHAMOMILLA, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, ACONITUM NAPELLUS, ANTIMONIUM CRUDUM, MEZEREUM, SEPIA, STAPHYSAGRIA, MAGNESIA PHOSPHORICA
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 3a117358-3c51-4870-9932-701ffe90e3f8
SPL ID 5572f8f5-96ae-4a68-82fd-d8f55ae59f77
Version 4
Effective date 2024-10-23
Source export date 2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:28:02 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Dental Pain openfda.brand_name generic name ACETICUM ACIDUM, CALENDULA OFFICINALIS, ZINGIBER OFFICINALE, BRYONIA (ALBA), COFFEA TOSTA, LEDUM PALUSTRE, PHOSPHORUS, PLANTAGO MAJOR, SPIGELIA ANTHELMIA, ARNICA MONTANA, CHAMOMILLA, HEPAR SULPHURIS CALCAREUM, HYPERICUM PERFORATUM, ACONITUM NAPELLUS, ANTIMONIUM CRUDUM, MEZEREUM, SEPIA, STAPHYSAGRIA, MAGNESIA PHOSPHORICA openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1523-1 openfda.package_ndc ndc product 43742-1523 openfda.product_ndc ndc11 package 43742152301 derived:openfda.package_ndc spl id 5572f8f5-96ae-4a68-82fd-d8f55ae59f77 id spl set id 3a117358-3c51-4870-9932-701ffe90e3f8 set_id unii 27YLU75U4W openfda.unii unii 877L01IZ0P openfda.unii unii 9H58JRT35E openfda.unii unii XK4IUX8MNB openfda.unii unii X2N6E405GV openfda.unii unii 00543AP1JV openfda.unii unii O80TY208ZW openfda.unii unii F79059A38U openfda.unii unii 18E7415PXQ openfda.unii unii QDL83WN8C2 openfda.unii unii Q40Q9N063P openfda.unii unii HF539G9L3Q openfda.unii unii W2469WNO6U openfda.unii unii WYT05213GE openfda.unii unii T7J046YI2B openfda.unii unii U0NQ8555JD openfda.unii unii G0R4UBI2ZZ openfda.unii unii C5529G5JPQ openfda.unii unii 1MBW07J51Q 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.