Cellpium shield sun bb

Manufacturer
MEDIPOST Co.,Ltd. | Kolmar Korea Co., Ltd.
Effective date
2016-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:27:59

Label at a glance#

ProductCellpium shield sun bb
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Label structure6 sections

Dosage and administration

Directions: The mild UV protectant protects skin from UV rays and urban pollutants and provides abundant moisture and nourishment to skin

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: TITANIUM DIOXIDE 11.00%, ETHYLHEXYL METHOXYCINNAMATE 6.50%, ETHYLHEXYL SALICYLATE 4.00%, ZINC OXIDE 3.91%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, TRIDECYL TRIMELLITATE, GLYCERIN, LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE, DIMETHICONE, C12-15 ALKYL BENZOATE, NIACINAMIDE, ISOPROPYL ISOSTEARATE, CAPRYLYL METHICONE, IRON OXIDES(CI 77492), DISTEARDIMONIUM HECTORITE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, MAGNESIUM SULFATE, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, DIMETHICONE CROSSPOLYMER, MICA, TALC, ALUMINUM HYDROXIDE, AMINOPROPYL DIMETHICONE, PHENOXYETHANOL, POLYMETHYLSILSESQUIOXANE, HUMAN CORD BLOOD CELL CONDITIONED MEDIA, IRON OXIDES(CI 77491), TRIBEHENIN, POLYGLYCERYL-6 POLYRICINOLEATE, STEARIC ACID, ALUMINA, ALLANTOIN, ETHYLHEXYLGLYCERIN, TOCOPHERYL ACETATE, FRAGRANCE, OCTYLDODECANOL, IRON OXIDES(CI 77499), SILICA, TRIETHOXYCAPRYLYLSILANE, ADENOSINE, SODIUM HYALURONATE, ECHIUM PLANTAGINEUM SEED OIL, CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES, TOCOPHEROL, MORINGA OLEIFERA SEED OIL, NELUMBO NUCIFERA CALLUS CULTURE EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT, ALCOHOL, PENTYLENE GLYCOL, HONEY EXTRACT, SODIUM HYDROXIDE, XANTHAN GUM

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: 1. If the following symptoms occur while using this product, discontinue use immediately and consult your dermatologist: (1). Red spots, swelling, itching, or irritation (2). If the application area develops the aforesaid symptoms after exposure to direct sunlight. 2. Do not apply on areas with injuries, eczema, or dermatitis. 3. Storage & Handling (1). Keep the cap closed after use. (2). Keep out of reach of children. (3). Keep away from direct sunlight and extreme high or low temperatures. 4. The UV protection factor of this product is measured according to the UV protection factor measurement method specified in the 「Regulation on the Review of Functional Cosmetics」. The rating of UVA protection factor is measured according to the method of measuring the UVA protection effect as specified in the「Regulation on the Review of Functional Cosmetics」. 5. Do not use on skin around the eyes. In case of contact with the eyes, wash off immediately with running water.

Directions

DESCRIPTION SECTION

Directions: The mild UV protectant protects skin from UV rays and urban pollutants and provides abundant moisture and nourishment to skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70506-110-012023-06-28C16284748780-19d75b9d1-0e9a-f424-e053-dadaa90a57cef8bb2eae-25da-4283-ab93-e966d11b1946
70506-110-012020-01-31C16284748780-19d75b9d1-0e9a-f424-e053-dadaa90a57cef8bb2eae-25da-4283-ab93-e966d11b1946

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70506-11070506-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
0b499d43-2f7f-4e2e-a6f7-4e7c4eab32f9f8bb2eae-25da-4283-ab93-e966d11b19462023-06-28WarningsExact identifier
spl set id: f8bb2eae-25da-4283-ab93-e966d11b1946

Reported adverse events (FAERS/openFDA)#

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