Home FDA labels 49ef1c5d-a07b-4bc0-9de1-dc40d8477d8f Zeel 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 Zeel
Generic name ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER
Manufacturer Biologische Heilmittel Heel
Product type HUMAN OTC DRUG
SPL set ID d5d7a2e5-a6ce-4a41-9430-1378023aa7d0
SPL ID 49ef1c5d-a07b-4bc0-9de1-dc40d8477d8f
Version 3
Effective date 2023-09-28
Source export date 2026-09-28
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:26:37 Harmonized routes table Harmonized routes TOPICAL
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 Zeel openfda.brand_name generic name ALPHA LIPOIC ACID, ARNICA MONTANA WHOLE,SUS SCROFA CARTILAGE, COENZYME A,SOLANUM DULCAMARA TOP,SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, NADIDE, SODIUM DIETHYL OXALACETATE,SUS SCROFA PLACENTA,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SILICON DIOXIDE,SULFUR,CORIANDER openfda.generic_name manufacturer name Biologische Heilmittel Heel openfda.manufacturer_name ndc package 51885-9489-8 openfda.package_ndc ndc product 51885-9489 openfda.product_ndc ndc11 package 51885948908 derived:openfda.package_ndc spl id 49ef1c5d-a07b-4bc0-9de1-dc40d8477d8f id spl set id d5d7a2e5-a6ce-4a41-9430-1378023aa7d0 set_id unii C8CV8867O8 openfda.unii unii KPS1B1162N openfda.unii unii O80TY208ZW openfda.unii unii SAA04E81UX openfda.unii unii 73Y7P0K73Y openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 6IO182RP7A openfda.unii unii 73ECW5WG2F openfda.unii unii 0U46U6E8UK openfda.unii unii 70FD1KFU70 openfda.unii unii N9288CD508 openfda.unii unii 6CA025Y4FG openfda.unii unii 118OYG6W3H openfda.unii unii 9928MC12VO openfda.unii unii 1OV56052IK 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 Warnings: For external use only. Do not use if pregnant or breast-feeding. Do not apply over open wounds or broken skin. In rare cases, allergic skin reactions may develop. Keep out of reach of children. If symptoms persist or worsen a healthcare provider should be consulted. If swallowed, get medical help or contact a Poison Control Center right away. Do not use if known sensitivity to Zeel® or any of its ingredients exists.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.