FDA label 1ad3a24f-b2cb-4189-aa4c-b4670bc8d657

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)

SPL set ID
3259fef2-b2e2-40aa-b383-601d65e982c4
SPL ID
1ad3a24f-b2cb-4189-aa4c-b4670bc8d657
Version
4
Effective date
2013-04-23
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:56:26

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 when using this product skin irritation may occur some medicines may interact with dimethicone, however, no specific interactions are known at this time Do not use if you are allergic to any ingredients listed if you have sensitive skin and/or are sensitive to Dimethicone do not use if you are pregnant, planning to become pregnant, or breast feeding if you have an open wound, burn, damaged or irritaed skin When using this product skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling should irritation occur lesson frequency of use avoid unnecessary sun exposure and use a 45 SPF sun screen when going outside Stop use and ask a doctor if: condition worsens symptoms last more than 7 days or clear up and occur again within a few days any of these severe effects occur; allergic reaction, irritation becomes severe i.e. persistent rash, hives, itching, burning, difficulty breathing, swelling

Reported adverse events (FAERS/openFDA)#

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