Folliculitis Treatment Cream

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
Folliculitis Treatment Cream
Generic name
BENZOYL PEROXIDE
Manufacturer
Guangzhou Hechuang Commercial Service Co.,Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
5a93f753-eb7d-ad11-e063-6294a90a6778
SPL ID
5a93f753-eb7c-ad11-e063-6294a90a6778
Version
1
Effective date
2026-09-01
Source export date
2026-10-27
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:59:08
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 Warnings For external use only. Do not use if you • have very sensitive skin • are sensitive to benzoyl peroxide When using this product do not get into eyes, lips, or mouth. If contact occurs, flush thoroughly with water. Avoid contact with hair and dyed fabrics, which may be bleached.

Reported adverse events (FAERS/openFDA)#

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