FDA label d4619054-0702-1fea-e053-2a95a90a39dc

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)

SPL set ID: addf8707-dc3d-9752-e053-2995a90a8fa8
SPL ID: d4619054-0702-1fea-e053-2a95a90a39dc
Version: 2
Effective date: 2021-12-30
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:48:22

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		d4619054-0702-1fea-e053-2a95a90a39dc	id
spl set id		addf8707-dc3d-9752-e053-2995a90a8fa8	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

DOLLY INTENSE LIGHTENING LOTION For external use only

Adverse event summaries are temporarily unavailable. Other product information remains available.