Dr. Sheffield Hydrocortisone Anti itch

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
Dr. Sheffield Hydrocortisone Anti itch
Generic name
HYDROCORTISONE
Manufacturer
Sheffield Pharmaceuticals LLC
Product type
HUMAN OTC DRUG
SPL set ID
71c9f2f4-2188-45eb-b55e-3856ac78070b
SPL ID
73503439-5ce2-480b-bf3f-9362a31c8e29
Version
4
Effective date
2023-10-30
Source export date
2026-10-30
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/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:55:30
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 genital itching if you have a vaginal discharge, consult a doctor. When using this product avoid contact with eyes do not begin the use of any other hydrocortisone product unless you have consulted a doctor. for external genital, feminine and anal itching do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, stop use, consult a doctor. do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if If condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and do not begin use of any other hydrocortisone product unless directed by 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.