Home FDA labels 3a627c71-037e-40c1-bd17-604157667dd2 BOLYM-EX Drops 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 BOLYM-EX Drops
Generic name BENZOIC ACID, FORMIC ACID, ARISTOLOCHIA CLEMATITIS ROOT, FERULA ASSA-FOETIDA RESIN, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CAPSELLA BURSA-PASTORIS, GALIUM APARINE, DAPHNE MEZEREUM BARK, AND PIPER METHYSTICUM ROOT
Manufacturer PEKANA Naturheilmittel GmbH
Product type HUMAN OTC DRUG
SPL set ID 77ec6ee5-1c22-4799-b582-1c32056b14ff
SPL ID 3a627c71-037e-40c1-bd17-604157667dd2
Version 5
Effective date 2022-12-23
Source export date 2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:45:47 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name BOLYM-EX Drops openfda.brand_name generic name BENZOIC ACID, FORMIC ACID, ARISTOLOCHIA CLEMATITIS ROOT, FERULA ASSA-FOETIDA RESIN, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, CALCIUM PHOSPHATE, UNSPECIFIED FORM, CAPSELLA BURSA-PASTORIS, GALIUM APARINE, DAPHNE MEZEREUM BARK, AND PIPER METHYSTICUM ROOT openfda.generic_name manufacturer name PEKANA Naturheilmittel GmbH openfda.manufacturer_name ndc package 59469-201-10 openfda.package_ndc ndc product 59469-201 openfda.product_ndc ndc11 package 59469020110 derived:openfda.package_ndc spl id 3a627c71-037e-40c1-bd17-604157667dd2 id spl set id 77ec6ee5-1c22-4799-b582-1c32056b14ff set_id unii 0YIW783RG1 openfda.unii unii X2N6E405GV openfda.unii unii BOW48C81XP openfda.unii unii 8SKN0B0MIM openfda.unii unii 1TH8Q20J0U openfda.unii unii ZY0NX0W00D openfda.unii unii 97Z1WI3NDX openfda.unii unii W9FZA51AS1 openfda.unii unii W0X9457M59 openfda.unii unii MA9CQJ3F7F openfda.unii unii Z4B6561488 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 Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.