Home FDA labels 854f9d21-a93d-43cc-90a6-3835e2f9f955 Lymphocil 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 Lymphocil
Generic name PHYTOLACCA DECANDRA, ARSENICUM IODATUM, AGRAPHIS NUTANS, APIUM GRAVEOLENS, ERIODICTYON CALIFORNICUM, ALLIUM SATIVUM, ERIGERON CANADENSIS, EUONYMUS ATROPURPUREUS, ACONITUM LYCOCTONUM, AETHIOPS ANTIMONIALIS, EUONYMUS EUROPAEUS, ABSINTHIUM, APIS MELLIFICA, CAUSTICUM, SANGUINARIA CANADENSIS, UVA URSI, CAPSICUM ANNUUM
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID b4372d5f-adf5-4316-8b73-3acb9a37b2f4
SPL ID 854f9d21-a93d-43cc-90a6-3835e2f9f955
Version 6
Effective date 2025-11-24
Source export date 2026-10-12
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:47:11 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Lymphocil openfda.brand_name generic name PHYTOLACCA DECANDRA, ARSENICUM IODATUM, AGRAPHIS NUTANS, APIUM GRAVEOLENS, ERIODICTYON CALIFORNICUM, ALLIUM SATIVUM, ERIGERON CANADENSIS, EUONYMUS ATROPURPUREUS, ACONITUM LYCOCTONUM, AETHIOPS ANTIMONIALIS, EUONYMUS EUROPAEUS, ABSINTHIUM, APIS MELLIFICA, CAUSTICUM, SANGUINARIA CANADENSIS, UVA URSI, CAPSICUM ANNUUM openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0002-1 openfda.package_ndc ndc product 75053-0002 openfda.product_ndc ndc11 package 75053000201 derived:openfda.package_ndc spl id 854f9d21-a93d-43cc-90a6-3835e2f9f955 id spl set id b4372d5f-adf5-4316-8b73-3acb9a37b2f4 set_id unii 00UK7646FG openfda.unii unii V1V998DC17 openfda.unii unii 11E6VI8VEG openfda.unii unii XCD2B9880O openfda.unii unii DD5FO1WKFU openfda.unii unii 16D08B0B9N openfda.unii unii F84709P2XV openfda.unii unii 3029988O2T openfda.unii unii EX75Q30TX6 openfda.unii unii 2Y7TIQ135H openfda.unii unii 3M5V3D1X36 openfda.unii unii 1G1EAA320L openfda.unii unii 7S82P3R43Z openfda.unii unii WJK59V19EW openfda.unii unii ZI0T668SF1 openfda.unii unii N9288CD508 openfda.unii unii 5F658PFU56 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: As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if: Symptoms persist for more than 7 days or worsen. Keep this and all medications out of reach of children. In case of accidental overdose, contact a medical professional or poison control center immediately. Do not use if seal is broken or missing. This Product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten, soy or milk derivatives.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.