Home FDA labels 482fcdd0-6d19-7b96-e063-6294a90a75f1 Teevodar 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 Teevodar
Generic name ALLANTOIN
Manufacturer PEER PHARM LTD.
Product type HUMAN OTC DRUG
SPL set ID 57a1b6d1-9439-462b-aeb9-ef806e572eaf
SPL ID 482fcdd0-6d19-7b96-e063-6294a90a75f1
Version 3
Effective date 2026-01-12
Source export date 2026-11-06
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/2026-11-06/968b7138703f8100b14008bced2b2a4531f4fab250b207279e9c05eb19608f40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 08:15:21 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 · 11 matching rows.
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 For external use only When using this product do not get into eyes Stop use and ask a doctor if contition worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.