DRMITSUI SILICONE SCAR REMOVER

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
DRMITSUI SILICONE SCAR REMOVER
Generic name
SILICONE
Manufacturer
Zhenping Renren Industry Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
4c2e9bd9-062d-670d-e063-6294a90ae1f4
SPL ID
4c2e9bd9-062e-670d-e063-6294a90ae1f4
Version
1
Effective date
2026-03-04
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:06:13
Harmonized routes table
Harmonized routes
CUTANEOUS, TRANSDERMAL

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 ●This product is intended for patients with hypertrophic scars who meet the indications outlined in this manual. ●Consumers may use this product as directed in this manual or as prescribed by a physician.For external use only. ●Discontinue use immediately if allergic reactions occur. ●Use within one year after opening (store in a cool,dry place). ●Consult a healthcare professional before using this product concurrently with other treatments or medications. Dispose of used product as regular household waste. ●Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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