Home FDA labels 490e2979-4bbb-4cae-9b78-5fd96ca2405c ThroatSpray 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 ThroatSpray
Generic name ECHINACEA (ANGUSTIFOLIA), EUGENIA CARYOPHYLLATA, GLYCERINUM, MYRRHA, SALVIA OFFICINALIS, SPILANTHES OLERACEA, THYMUS SERPYLLUM, BAPTISIA TINCTORIA, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, LACHESIS MUTUS, MERCURIUS SOLUBILIS, HEPAR SULPHURIS CALCAREUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 125ffbf4-681e-451c-a96d-0b6416619474
SPL ID 490e2979-4bbb-4cae-9b78-5fd96ca2405c
Version 1
Effective date 2025-04-29
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:29 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 ThroatSpray openfda.brand_name generic name ECHINACEA (ANGUSTIFOLIA), EUGENIA CARYOPHYLLATA, GLYCERINUM, MYRRHA, SALVIA OFFICINALIS, SPILANTHES OLERACEA, THYMUS SERPYLLUM, BAPTISIA TINCTORIA, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, LACHESIS MUTUS, MERCURIUS SOLUBILIS, HEPAR SULPHURIS CALCAREUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0737-1 openfda.package_ndc ndc product 44911-0737 openfda.product_ndc ndc11 package 44911073701 derived:openfda.package_ndc spl id 490e2979-4bbb-4cae-9b78-5fd96ca2405c id spl set id 125ffbf4-681e-451c-a96d-0b6416619474 set_id unii 86H4S6K51N openfda.unii unii 11E6VI8VEG openfda.unii unii 324Y4038G2 openfda.unii unii K48IKT5321 openfda.unii unii PDC6A3C0OX openfda.unii unii 1O11RD9U53 openfda.unii unii VB06AV5US8 openfda.unii unii ZW3Z11D0JV openfda.unii unii WQZ3G9PF0H openfda.unii unii VSW71SS07I openfda.unii unii 065C5D077J openfda.unii unii 5EF0HWI5WU openfda.unii unii 7S82P3R43Z openfda.unii unii JC71GJ1F3L 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 breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place. Warning - Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by physician.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.