POZCOS PO CC Cream

Manufacturer
Chang Ha Co.,Ltd | GreenCos co.,Ltd
Effective date
2021-02-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:53:55

Label at a glance#

ProductPOZCOS PO CC Cream
Active ingredientOCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Dosage and administration

• Evenly apply the appropriate amount of cream on your face • Apply liberally and evenly 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating • 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 value of 15 or higher ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene, Titanium dioxide, Zinc oxide

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin

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

Stop use and ask doctor if rash occurs

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Evenly apply the appropriate amount of cream on your face

• Apply liberally and evenly 15 minutes before sun exposure

• Reapply at least every 2 hours

• Use a water-resistant sunscreen if swimming or sweating

• 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 value of 15 or higher and other sun protection measures including:

• Limit time in the sun, especially from 10 a.m.-2 p.m.

• Wear long-sleeved shirts, pants, hats, and sunglasses

• Children under 6 months of age: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE, CETYL ETHYLHEXANOATE, ZINC OXIDE, PHENYL TRIMETHICONE, DIPROPYLENE GLYCOL, CETYL PEG/PPG-10/1 DIMETHICONE, CYCLOPENTASILOXANE, CAPRYLIC/CAPRIC TRIGLYCERIDE, ETHYLHEXYL SALICYLATE, DIMETHICONE, 1,2-HEXANEDIOL, LOESS, NIACINAMIDE, OCTOCRYLENE, QUATERNIUM-18 BENTONITE, BEESWAX, 4-METHYLBENZYLIDENE CAMPHOR, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, GLYCERIN, SORBITAN OLIVATE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, HEXYL LAURATE, POLYGLYCERYL-4 ISOSTEARATE, OZOKERITE, POLYGLYCERYL-2 SESQUIISOSTEARATE, CYCLOHEXASILOXANE, MINERAL OIL, PHENOXYETHANOL, ALOE BARBADENSIS LEAF EXTRACT, GINKGO BILOBA LEAF EXTRACT, TRIETHOXYCAPRYLYLSILANE, MAGNESIUM STEARATE, POLYESTER-1, SILICA DIMETHYL SILYLATE, MICROCRYSTALLINE WAX, ALUMINUM STEARATE, FRAGRANCE, ADENOSINE, QUARTZ, BUTYLENE GLYCOL, CENTELLA ASIATICA EXTRACT, DISODIUM EDTA, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL, ALLANTOIN, SODIUM HYALURONATE, ALUMINUM HYDROXIDE, PENTYLENE GLYCOL, CAPRYLYL GLYCOL, CI 77492, CI 77491, CI 77499, MICA

​POZCOS PO CC Cream-30g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30g30g

Products#

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DailyMed product names page 1 of 2 · 44 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81397-30181397-301-01, 81397-301-02

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 42 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
c39a11df-9dcc-07a1-e053-2a95a90a313cb9647f15-07f6-1f95-e053-2995a90ae1c82021-05-31WarningsExact identifier
spl set id: b9647f15-07f6-1f95-e053-2995a90ae1c8

Reported adverse events (FAERS/openFDA)#

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