Maximum Strength Hydrocortisone

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
Maximum Strength Hydrocortisone
Generic name
HYDROCORTISONE
Manufacturer
DLC Laboratories, Inc
Product type
HUMAN OTC DRUG
SPL set ID
caf50f12-f35c-4e9e-8ef7-3b0c84e225ee
SPL ID
47d50931-ec8a-bab5-e063-6394a90a6e6b
Version
6
Effective date
2026-01-07
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:35:01
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use for the treatment of diaper rash. Consult a doctor. for external feminine itching if you have a vaginal discharge. Consult a doctor. When using this product avoid contact with the eyes do not use more than directed unless told to do so by a doctor do not put this product into rectum by using fingers or any mechanical device or applicator Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Do not begin use of any other hydrocortisone product unless you have consulted a doctor. rectal bleeding occurs KEEP OUT OF THE REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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