Dermeleve Anti Itch Scalp Serum

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
Dermeleve Anti Itch Scalp Serum
Generic name
ALUMINUM ACETATE
Manufacturer
Advanced Derm Solutions LLC
Product type
HUMAN OTC DRUG
SPL set ID
c53e075e-b9cb-4434-a38d-2cf3dae0b438
SPL ID
4092aaf5-3e61-694d-e063-6394a90aa64e
Version
6
Effective date
2025-10-07
Source export date
2026-09-28
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/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:38:09
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 . Avoid contact with eyes. Do not apply to open wounds. STOP USE and ask a doctor if condition worsens or symptoms persist for more than seven days. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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