Home FDA labels d2950c66-ed0a-430f-93c9-e0c79b20f6b3 Itch Formula 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 Itch Formula
Generic name CALENDULA OFFICINALIS, APIS MELLIFICA, NATRUM MURIATICUM, URTICA URENS, HISTAMINUM HYDROCHLORICUM, LEDUM PALUSTRE, SULPHUR, COPAIVA OFFICINALIS, CANTHARIS, CROTON TIGLIUM, GRAPHITES, MEZEREUM, PETROLEUM, RHUS VENENATA, STAPHYSAGRIA, ANTIPYRINUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 79c21a7b-ffb7-4b0d-a702-8aec0463be81
SPL ID d2950c66-ed0a-430f-93c9-e0c79b20f6b3
Version 2
Effective date 2024-09-11
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 06:28:13 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Itch Formula openfda.brand_name generic name CALENDULA OFFICINALIS, APIS MELLIFICA, NATRUM MURIATICUM, URTICA URENS, HISTAMINUM HYDROCHLORICUM, LEDUM PALUSTRE, SULPHUR, COPAIVA OFFICINALIS, CANTHARIS, CROTON TIGLIUM, GRAPHITES, MEZEREUM, PETROLEUM, RHUS VENENATA, STAPHYSAGRIA, ANTIPYRINUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1413-1 openfda.package_ndc ndc product 43742-1413 openfda.product_ndc ndc11 package 43742141301 derived:openfda.package_ndc spl id d2950c66-ed0a-430f-93c9-e0c79b20f6b3 id spl set id 79c21a7b-ffb7-4b0d-a702-8aec0463be81 set_id unii 877L01IZ0P openfda.unii unii X2N6E405GV openfda.unii unii 3POA0Q644U openfda.unii unii 00543AP1JV openfda.unii unii T3CHA1B51H openfda.unii unii 4QQN74LH4O openfda.unii unii 18E7415PXQ openfda.unii unii Y3VW699H96 openfda.unii unii 3Q034RO3BT openfda.unii unii 451W47IQ8X openfda.unii unii 70FD1KFU70 openfda.unii unii 0HK2GZK66E openfda.unii unii 7S82P3R43Z openfda.unii unii 1VH544O5AT openfda.unii unii 1C89KKC04E 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: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "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.