FDA.reportPublic FDA data

POZCOS PO CC Cream

Manufacturer
Chang Ha Co.,Ltd | GreenCos co.,Ltd
Effective date
2021-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:55:45

Label at a glance#

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

Indications and uses

• Helps prevent sunburn

Dosage and administration

• Smoothly and evenly apply the appropriate amount of cream after cleansing and base makeup • 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 Spe...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene, Titanium Dioxide, Zinc Oxide

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

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

• Smoothly and evenly apply the appropriate amount of cream after cleansing and base makeup

• 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, PORTULACA OLERACEA EXTRACT, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, HEXYL LAURATE, OZOKERITE, 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, LIMONENE, LINALOOL, ALUMINUM HYDROXIDE, BUTYLPHENYL METHYLPROPIONAL, HEXYL CINNAMAL, CAPRYLYL GLYCOL, CI 77492, CI 77491, CI 77499, MICA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

40g40g

Products#

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

DailyMed product names page 1 of 2 · 48 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81397-20181397-201-01, 81397-201-02

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 46 matching rows.

Name, UNII, Kind table
NameUNIIKind
BEMOTRIZINOLPWZ1720CBHIACT
GLYCERINPDC6A3C0OXIACT
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TIACT
PORTULACA OLERACEA WHOLED5J3623SV2IACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
HEXYL LAURATE4CG9F9W01QIACT
CYCLOMETHICONE 6XHK3U310BAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GINKGO19FUJ2C58TIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
MAGNESIUM STEARATE70097M6I30IACT
NIACINAMIDE25X51I8RD4IACT
BENTOQUATAM7F465U79Q1IACT
ENZACAMENE8I3XWY40L9IACT
SORBITAN OLIVATEMDL271E3GRIACT
OCTINOXATE4Y5P7MUD51IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
ALUMINUM STEARATEU6XF9NP8HMIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CENTELLA ASIATICA7M867G6T1UIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
MICAV8A1AW0880IACT
PEG-8 BEESWAX3C1QUF1TIRIACT
OCTISALATE4X49Y0596WIACT
DIMETHICONE 100RO266O364UIACT
OCTOCRYLENE5A68WGF6WMACTIB
CETYL ETHYLHEXANOATE134647WMX4IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CERESINQ1LS2UJO3AIACT
MINERAL OILT5L8T28FGPIACT
ALOE VERA LEAFZY81Z83H0XIACT
SILICA DIMETHYL SILYLATEEU2PSP0G0WIACT
ADENOSINEK72T3FS567IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
FERRIC OXIDE RED1K09F3G675IACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT

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
c34b1a74-eb4e-64a2-e053-2995a90aac0cb83deffa-e80d-a06a-e053-2995a90a3db92021-05-27WarningsExact identifier
spl set id: b83deffa-e80d-a06a-e053-2995a90a3db9

Reported adverse events (FAERS/openFDA)#

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