Home FDA labels 4604f3de-7763-ddaa-e063-6394a90a78d0 Chronic Fatigue Therapy 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 Chronic Fatigue Therapy
Generic name EPINEPHRINE, GOLD, CHELIDONIUM MAJUS, ECHINACEA, GINKGO, HELLEBORUS NIGER, PHOSPHORIC ACID, SCUTELLARIA LATERIFLORA, THUJA OCCIDENTALIS
Manufacturer TRP Company
Product type HUMAN OTC DRUG
SPL set ID 751334b8-f21b-3f94-e053-2a91aa0a9bb9
SPL ID 4604f3de-7763-ddaa-e063-6394a90a78d0
Version 2
Effective date 2025-12-15
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:16 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 · 17 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Chronic Fatigue Therapy openfda.brand_name generic name EPINEPHRINE, GOLD, CHELIDONIUM MAJUS, ECHINACEA, GINKGO, HELLEBORUS NIGER, PHOSPHORIC ACID, SCUTELLARIA LATERIFLORA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name TRP Company openfda.manufacturer_name ndc package 17312-170-14 openfda.package_ndc ndc product 17312-170 openfda.product_ndc ndc11 package 17312017014 derived:openfda.package_ndc spl id 4604f3de-7763-ddaa-e063-6394a90a78d0 id spl set id 751334b8-f21b-3f94-e053-2a91aa0a9bb9 set_id unii 7E889U5RNN openfda.unii unii 608DGJ6815 openfda.unii unii 1NT28V9397 openfda.unii unii 79Y1949PYO openfda.unii unii YKH834O4BH openfda.unii unii 4N9P6CC1DX openfda.unii unii 7BP4DH5PDC openfda.unii unii 19FUJ2C58T openfda.unii unii E4GA8884NN 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 A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur . Stop use Stop use and ask a doctor if: • You experience worsening of symptoms. • Symptoms last longer than 7 days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.