FDA.reportPublic FDA data

Alumier MD Intensive Recovery

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
Alumier MD Intensive Recovery
Generic name
HYDROCORTISONE
Manufacturer
Alumier Labs
Product type
HUMAN OTC DRUG
SPL set ID
d9b79ea1-6558-543c-e053-2995a90ae53e
SPL ID
3bb3d148-e68d-658a-e063-6394a90a0301
Version
3
Effective date
2025-08-06
Source export date
2026-08-01
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/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:04:11
Harmonized routes table
Harmonized routes
TOPICAL

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 for the treatment of diaper rash, except on the advice of a physician When using this product avoid contact with eyes, do not use in or around the eyes Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clears up and occurs again within a few days. Do not begin use of any other hydrocortisone product unless directed by a physician. Keep out of reach of children. If swallowed, call a Poison Control Centre or get medical help right away.