Plushmallow SUNSTICK

Manufacturer
COSNINE Inc
Effective date
2019-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:10

Label at a glance#

ProductPlushmallow SUNSTICK
Active ingredientOCTOCRYLENE, AVOBENZONE, HOMOSALATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Octocrylene, Homosalate, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane

INACTIVE INGREDIENT SECTION

Dimethicone
Polyethylene
Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer
Ozokerite
Acrylates Copolymer
Silica
Neopentyl Glycol Diheptanoate
Butyloctyl Salicylate
Cetyl Ethylhexanoate
HDI/Trimethylol Hexyllactone Crosspolymer
Polymethyl Methacrylate
Cetyl Alcohol
Tocopheryl Acetate
Caprylic/Capric Triglyceride
Citrus Aurantium Dulcis (Orange) Peel Oil
Geranium Maculatum Oil
Lavandula Angustifolia (Lavender) Oil
Citrus Aurantium Bergamia (Bergamot) Fruit Oil
Cymbopogon Martini Oil
Anthemis Nobilis Flower Oil

OTC - PURPOSE SECTION

protects the skin from harmful UV rays (SPF50+ PA++++)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Evenly apply a moderate amount
on areas exposed to sunlight during the last step of
your skincare routine. Carry it with you at all times
to frequently apply to necessary areas (face, body).

WARNINGS SECTION

1. While using this product , if there
is any abnormal symptoms or side effect such as red spot,
swelling or itching, please consult with dermatologist.
2. Do not use in areas with wounds 3. Instructions for sto
-rage and usage. (i) Keep out of reach of infants and chil
-dren (ii) Store it in a place away from direct sunlight

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73330-0001-12022-01-28C16284748780-1d6a99b39-509b-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73330-0001-1Plushmallow SUNSTICK19 g in 1 PACKAGESTICK191

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73330-0001PLUSHMALLOW SUNSTICK (OCTOCRYLENE, HOMOSALATE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) STICK [COSNINE INC]1Legacy NDC, 1 package rows20190831_9165b262-3418-4113-e053-2a95a90adaf1.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73330-000173330-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
9165b430-28d8-513d-e053-2a95a90a38149165b262-3418-4113-e053-2a95a90adaf12019-08-31WarningsExact identifier
spl id: 9165b430-28d8-513d-e053-2a95a90a3814
spl set id: 9165b262-3418-4113-e053-2a95a90adaf1

Reported adverse events (FAERS/openFDA)#

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