SORARESAL

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
SORARESAL
Generic name
SALICYLIC ACID
Manufacturer
Summer Herbal Inc.
Product type
HUMAN OTC DRUG
SPL set ID
af734362-057b-4011-bf4e-c4e4dd67f68c
SPL ID
d43790bf-7043-408e-829f-08edb70ffdbd
Version
12
Effective date
2024-09-03
Source export date
2026-10-30
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:38:50
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. Do not use • on open wounds, infected or cracked skin. • if you are sensitive or allergic to any of the ingredients used in this product. Ask a doctor before use if you have a condition that covers a large area of the body. When using this product • avoid contact with the eyes and if contact occurs, rinse eyes thoroughly with water. • avoid contact with the mouth, genitals and mucous membranes. • avoid direct sunlight after use. 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.