FDA.reportPublic FDA data

IM DERMA RELIEF SUNSTICK

Manufacturer
Normalest Co., Ltd.
Effective date
2019-12-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:45

Label at a glance#

ProductIM DERMA RELIEF SUNSTICK
Active ingredientOCTINOXATE, OCTOCRYLENE, OCTISALATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

reliefrelief

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

OTC - ASK DOCTOR SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

OTC - WHEN USING SECTION

DOSAGE & ADMINISTRATION SECTION

OTHER SAFETY INFORMATION

WARNINGS SECTION

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72284-0010-12022-01-28C16284748780-1d6a99b39-3683-a426-e053-dadaa90af4c2SUNTIQUE I'M DERMA RELIEF SUNSTICK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72284-0010-1IM DERMA RELIEF SUNSTICK15 g in 1 CONTAINERSTICK151
72284-0010-1IM DERMA RELIEF SUNSTICK1 in 1 BOXSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72284-0010IM DERMA RELIEF SUNSTICK (OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE) STICK [NORMALEST CO., LTD.]1Legacy NDC, 2 package rows20191205_98f10868-1d00-cfc7-e053-2995a90a2873.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72284-001072284-0010-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYIACT
CENTELLA ASIATICA7M867G6T1UIACT
DIMETHICONE92RU3N3Y1OIACT
PARAFFINI9O0E3H2ZEIACT
TRIETHYLHEXANOIN7K3W1BIU6KIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE75D21FL1PIIACT
OCTINOXATE4Y5P7MUD51ACTIB
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
CANDELILLA WAXWL0328HX19IACT
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMEREG97988M5QIACT
BEMOTRIZINOLPWZ1720CBHIACT
DIPROPYLENE GLYCOLE107L85C40IACT
GLYCERINPDC6A3C0OXIACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
WATER059QF0KO0RIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
POLYGLYCERYL-10 OLEATE55C81W76DHIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
ADENOSINEK72T3FS567IACT
MADECASSOSIDECQ2F5O6YIYIACT
PENTYLENE GLYCOL50C1307PZGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYALURONATE SODIUMYSE9PPT4THIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
98f0f51a-10e0-386b-e053-2a95a90a0fd998f10868-1d00-cfc7-e053-2995a90a28732019-12-05Exact identifier
spl id: 98f0f51a-10e0-386b-e053-2a95a90a0fd9
spl set id: 98f10868-1d00-cfc7-e053-2995a90a2873

Reported adverse events (FAERS/openFDA)#

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