Home FDA labels 5738b40a-8261-9a9e-e063-6394a90a1f15 Dermasporin 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 Dermasporin
Generic name LANOLIN
Manufacturer Marie's Original Formulas LLC
Product type HUMAN OTC DRUG
SPL set ID 562f40aa-eeec-2b7c-e063-6294a90ad68d
SPL ID 5738b40a-8261-9a9e-e063-6394a90a1f15
Version 2
Effective date 2026-07-22
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 05:26:40 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 · 10 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. Do not use • On deep or puncture wounds. • On animal bites. • On serious burns. When using this product • Do not get into eyes. Stop use and ask a doctor if • Condition worsens. • Symptoms last more than 7 days or clear up and occur again within a few days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.