FDA label 46dd68de-8746-1619-e054-00144ff8d46c

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: dc6eb3c1-c793-496d-9d94-ee9a6c56f051
SPL ID: 46dd68de-8746-1619-e054-00144ff8d46c
Version: 4
Effective date: 2017-01-24
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:30:39

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		46dd68de-8746-1619-e054-00144ff8d46c	id
spl set id		dc6eb3c1-c793-496d-9d94-ee9a6c56f051	set_id

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. Avoid contact with the eyes. When using this product When using this product Do not use otherwise than as directed. Do not apply to wounds or damaged skin. Do not bandage tightly. Stop use and ask a doctor if Redness is present. Excessive irritation of skin develops. Condition worsens symptoms persist for more than 7 days or clean up and occur again within a few days If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children if swallowed get medical help contact Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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