Seacall Hydrocortisone Ointment.

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
Seacall Hydrocortisone Ointment.
Generic name
SEACALL HYDROCORTISONE OINTMENT
Manufacturer
Guangdong Quadrant Ecological Technology Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
3616980a-03dc-deba-e063-6394a90a6ce7
SPL ID
3616980a-03dd-deba-e063-6394a90a6ce7
Version
1
Effective date
2025-05-26
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:46
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. ·Not for infants. ·Use with caution in pregnant and lactating women. ·Prohibited for those who are allergic to this product. Allergic persons should be cautious. ·Prohibit the use of this product when the properties of the product have changed. ·Should not be used on a large scale and for a long time.

Reported adverse events (FAERS/openFDA)#

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