Denorex Multi-Symptom Anti-Dandruff

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
Denorex Multi-Symptom Anti-Dandruff
Generic name
SALICYLIC ACID
Manufacturer
Neoteric Cosmetics, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
4e904a6b-a732-558b-e063-6294a90ac642
SPL ID
4e9052bd-27ac-55d3-e063-6294a90a4e3a
Version
1
Effective date
2026-04-01
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 19:45:14
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. Ask a doctor before use if you have a condition that covers a large area of body. When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor If condition worsens or does not improve after regular use of this product as directed. 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.