FDA.reportPublic FDA data

SIIMUNANA Bio Sun Stick

Manufacturer
Guangzhou Simunana Biotechnology Co., Ltd.
Effective date
2024-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:15:44

Label at a glance#

ProductSIIMUNANA Bio Sun Stick
Active ingredientOCTISALATE, MENTHOL
Label structure9 sections

Storage and handling

SHELE LIFE:3 years

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ETHYLHEXYL SALICYLATE 4.5%
MENTHOLUM 1%

OTC - PURPOSE SECTION

MOISTURIZING AND ISOLATING
SUNSCREEN AND SKIN BEAUTIFICATION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION

INDICATIONS & USAGE SECTION

MOISTURIZING AND ISOLATING
SUNSCREEN AND SKIN BEAUTIFICATION

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

Apply evenly on the skin

STORAGE AND HANDLING SECTION

SHELE LIFE:3 years

INACTIVE INGREDIENT SECTION

POLYISOBUTENE
ETHYLHEXYL PALMITATE
ISOHEXADECANE
OZOKERITE
TRIETHYLHEXANOIN
MICA
OCTOCRYLENE
TRIDECYL TRIMELLITATE
SYNTHETIC WAX
ISONONYL ISONONANOATE

MICROCRYSTALLINE WAX

TITANIUM DIOXIDE
BEESWAX

SILICA
TRIETHOXYCAPRYLYLSILANE
DIMETHICONE
CI 77891
CI 15850
CI 47005

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84565-001-012025-07-29C16284748780-13b156c62-29e9-fb37-e063-e6dba90a4e07SIIMUNANA Bio Sun Stick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84565-001-01SIIMUNANA Bio Sun Stick20 g in 1 BOTTLECREAM, AUGMENTED201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84565-001SIIMUNANA BIO SUN STICK (ETHYLHEXYL SALICYLATE, MENTHOL) CREAM, AUGMENTED [GUANGZHOU SIMUNANA BIOTECHNOLOGY CO., LTD.]11 package rows20240723_1dd22c4f-1692-a7a5-e063-6294a90abd27.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84565-00184565-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
MICROCRYSTALLINE WAXXOF597Q3KYIACT
YELLOW WAX2ZA36H0S2VIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
2-ETHYLHEXYL ISOHEXADECANOATEE1RR6O4O9SIACT
CERESINQ1LS2UJO3AIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
ISONONYL ISONONANOATES4V5BS6GCXIACT
D&C RED NO. 6481744AI4OIACT
TRIETHYLHEXANOIN7K3W1BIU6KIACT
OCTISALATE4X49Y0596WACTIB
ISOCETANE8LP0677305IACT
DIMETHICONE92RU3N3Y1OIACT
OCTOCRYLENE5A68WGF6WMIACT
MENTHOLL7T10EIP3AACTIB
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
TRIDECYL TRIMELLITATEFY36J270ESIACT

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
1dd22c4f-1693-a7a5-e063-6294a90abd271dd22c4f-1692-a7a5-e063-6294a90abd272024-07-22WarningsExact identifier
spl id: 1dd22c4f-1693-a7a5-e063-6294a90abd27
spl set id: 1dd22c4f-1692-a7a5-e063-6294a90abd27

Reported adverse events (FAERS/openFDA)#

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