KIWIGLOW VEGAN JEJU LOTUS FLOWER WATERY NON-NANO SUNSCREEN

Manufacturer
VANDA BNH INC. | Kolmar Korea Co., Ltd.
Effective date
2023-04-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:33:15

Label at a glance#

ProductKIWIGLOW VEGAN JEJU LOTUS FLOWER WATERY NON-NANO SUNSCREEN
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 17%..………………..……Sunscreen

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours


Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses

Ask a doctor to use for children under 6 months

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

When using this product, keep out of eyes. Rinse with water to remove

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

WATER, CYCLOHEXASILOXANE, PROPANEDIOL, BUTYLOCTYL SALICYLATE, PROPYLHEPTYL CAPRYLATE, POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, ISODODECANE, CAPRYLYL METHICONE, METHYL METHACRYLATE CROSSPOLYMER, METHYL TRIMETHICONE, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, TRIETHOXYCAPRYLYLSILANE, 1,2-HEXANEDIOL, POLYGLYCERYL-DIPOLYHYDROXYSTEARATE, POLYMETHYLSILSESQUIOXANE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, BUTYLENE GLYCOL, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, FRAGRANCE, ETHYLHEXYLGLYCERIN, SODIUM HYALURONATE, NELUMBIUM SPECIOSUM FLOWER EXTRACT, TOCOPHEROL, PANTHENOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, XYLITYLGLUCOSIDE, ANHYDROXYLITOL, GANODERMA LUCIDUM (MUSHROOM) EXTRACT, XYLITOL, GLYCERIN, GLUCOSE, CAMELLIA SINENSIS LEAF EXTRACT, CENTELLA ASIATICA EXTRACT, XANTHAN GUM, HYDROLYZED HYALURONIC ACID, SODIUM ACETYLATED HYALURONATE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83362-00183362-001-01, 83362-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 36 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
0d91c16d-4c45-8dd0-e063-6394a90a358d5eb50dc7-0128-4f2d-9706-49df582e0c752023-12-28WarningsExact identifier
spl set id: 5eb50dc7-0128-4f2d-9706-49df582e0c75

Reported adverse events (FAERS/openFDA)#

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