Home FDA labels f33f0e2c-2276-45b1-b697-60678cff40b0 MCAS Support 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 MCAS Support
Generic name APIS MELLIFICA, ANTIMONIUM CRUDUM, ASCORBICUM ACIDUM, BOVISTA, CARBOLICUM ACIDUM, CHAMOMILLA, CORTISONE ACETICUM, GINKGO BILOBA, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, QUERCETIN, RHUS TOX, SCUTELLARIA LATERIFLORA, STOMACH (SUIS), URTICA URENS
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID af3d5f8f-6f24-4045-8730-c776ff54bcc4
SPL ID f33f0e2c-2276-45b1-b697-60678cff40b0
Version 1
Effective date 2026-06-24
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 05:15:22 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name MCAS Support openfda.brand_name generic name APIS MELLIFICA, ANTIMONIUM CRUDUM, ASCORBICUM ACIDUM, BOVISTA, CARBOLICUM ACIDUM, CHAMOMILLA, CORTISONE ACETICUM, GINKGO BILOBA, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, NATRUM MURIATICUM, QUERCETIN, RHUS TOX, SCUTELLARIA LATERIFLORA, STOMACH (SUIS), URTICA URENS openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2550-1 openfda.package_ndc ndc product 43742-2550 openfda.product_ndc ndc11 package 43742255001 derived:openfda.package_ndc spl id f33f0e2c-2276-45b1-b697-60678cff40b0 id spl set id af3d5f8f-6f24-4045-8730-c776ff54bcc4 set_id unii T0920P9Z9A openfda.unii unii K2A74U428F openfda.unii unii 3POA0Q644U openfda.unii unii 883WKN7W8X openfda.unii unii F79059A38U openfda.unii unii 451W47IQ8X openfda.unii unii IHN2NQ5OF9 openfda.unii unii PQ6CK8PD0R openfda.unii unii 339NCG44TV openfda.unii unii 6IO182RP7A openfda.unii unii 7BP4DH5PDC openfda.unii unii 9IKM0I5T1E openfda.unii unii 19FUJ2C58T openfda.unii unii 7S82P3R43Z openfda.unii unii G0R4UBI2ZZ openfda.unii unii 6EC706HI7F 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.