FDA label 4f028fcb-f4af-bb14-e063-6294a90a4fd2

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
4f028fcb-f4ae-bb14-e063-6294a90a4fd2
SPL ID
4f028fcb-f4af-bb14-e063-6294a90a4fd2
Version
1
Effective date
2026-04-09
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:28:58

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

For external use only. Do not use if you are allergic to Amnica Montana or any of the ingredients. Avoid contact with eyes, mucous membranes, or broken skin. Stop use and ask a doctor if condition worsens or symptoms persist for more than 3 days. Keep out of reach of children. In case of ingestion, seek medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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