Walgreens Scalp 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
Walgreens Scalp Itch Relief
Generic name
HYDROCORTISONE
Manufacturer
Walgreens
Product type
HUMAN OTC DRUG
SPL set ID
34952272-1f9e-c642-e063-6394a90ae2bd
SPL ID
52f753e8-3334-be85-e063-6394a90ac7df
Version
2
Effective date
2026-05-29
Source export date
2026-10-27
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:45:20
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

For external use only. Use only as directed. Flammable . Keep away from fire or flame. Do not use for the treatment of diaper rash; consult a doctor if you are allergic to any ingredient in this product. When using this produc t avoid contact with eyes, do not use more than directed unless told to 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, do not use this or any other hydrocortisone product unless you have asked a doctor.

Reported adverse events (FAERS/openFDA)#

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