Cortizone 10 Feminine Itch Relief

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
Cortizone 10 Feminine Itch Relief
Generic name
HYDROCORTISONE
Manufacturer
Chattem, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
c0c0c1fb-43c9-4903-bb3b-f0885619b8cc
SPL ID
901fbbc8-7ebe-4b33-a3cc-4a14896417b1
Version
4
Effective date
2026-01-14
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 05:35:02
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. Consult a doctor. ■ if you have vaginal discharge. Consult a doctor. ■ if you are allergic to any ingredient in this product When using this product ■ avoid contact with eyes ■ do not use more than directed unless told to do so by a doctor Stop use and ask a doctor if ■ condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor Keep out of 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.