Dr. Sayman Salve

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
Dr. Sayman Salve
Generic name
SALVE
Manufacturer
Sheffield Pharmaceuticals LLC
Product type
HUMAN OTC DRUG
SPL set ID
18bdcd0c-9c81-47e1-ae24-2239ff8fd066
SPL ID
c45b2ae3-b31c-4ac3-8f89-fc8a60d7fd99
Version
2
Effective date
2023-10-24
Source export date
2026-10-22
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-22/e5f4d4a4616a7a32d70e04156e4d0babf78b8f6273b85bc55228fdc2c537c220/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run
20261023T001338Z
Imported at
2026-10-23 00:42:05
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 Sun Alert: limiting sun exposure,wearing protectvie clothing,and usingsunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if condition worsens or symptoms last more than seven days or clear up and occur again within a few days. Don't use on deep/ puncture wounds,animal bites or serious burns.

Reported adverse events (FAERS/openFDA)#

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