FDA.reportPublic FDA data

KONEUK SUNSCREEN SPF50

Manufacturer
Guangzhou Meixi Biotechnology Co., Ltd.
Effective date
2026-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:11

Label at a glance#

ProductKONEUK SUNSCREEN SPF50
Active ingredientOCTOCRYLENE, HOMOSALATE, TITANIUM DIOXIDE, AVOBENZONE, ENSULIZOLE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

HOMOSALATE,OCTOCRYLENE,AVOBENZONE,ENSULIZOLE,TITANIUM DIOXIDE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children section

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

keep out reach of children

INACTIVE INGREDIENT SECTION

WATER,CETYL ETHYLHEXANOATE,ETHYLHEXYL STEARATE,GLYCERIN,DIBUTYL ADIPATE,DIPROPYLENE GLYCOL

DOSAGE & ADMINISTRATION SECTION

Apply to the palms, rub onto the skin, used for sun protection

INDICATIONS & USAGE SECTION

Apply to the palms, rub onto the skin, used for sun protection

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84167-323-03KONEUK SUNSCREEN SPF505 in 1 BOXCREAM51
84167-323-03KONEUK SUNSCREEN SPF501 in 1 BOTTLECREAM11

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84167-32384167-323-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPANEDIOL5965N8W85TIACT
TRIETHANOLAMINE9O3K93S3TKIACT
C12-20 ALKYL GLUCOSIDEK67N5Z1RUAIACT
OCTOCRYLENE5A68WGF6WMACTIB
GLYCERINPDC6A3C0OXIACT
HOMOSALATEV06SV4M95SACTIB
2-BROMO-4'-HYDROXYACETOPHENONE6H0QU4I6BAIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
CITRIC ACID2968PHW8QPIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
FRAGRANCE 135765EM498GW35IACT
DIBUTYL ADIPATEF4K100DXP3IACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
PEG-100 STEARATEYD01N1999RIACT
CETYL ETHYLHEXANOATE134647WMX4IACT
CALCIUM DISODIUM EDTA8U5D034955IACT
DISODIUM ALPHA-TOCOPHERYL PHOSPHATE, DL-35ZC9LRM4UIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
AVOBENZONEG63QQF2NOXACTIB
ALLANTOIN344S277G0ZIACT
GLYCERYL STEARATE230OU9XXE4IACT
ENSULIZOLE9YQ9DI1W42ACTIB
XANTHAN GUMTTV12P4NEEIACT
WATER059QF0KO0RIACT
DIPROPYLENE GLYCOLE107L85C40IACT
C14-22 ALCOHOLSB1K89384RJIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
SODIUM HYDROXIDE55X04QC32IIACT
POLYSORBATE 60CAL22UVI4MIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT

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
KONEUK SUNSCREEN SPF50KONEUK SUNSCREEN SPF50Guangzhou Meixi Biotechnology Co., Ltd.48dd7f6e-2a4d-2c92-e063-6294a90a42552026-01-20WarningsExact identifier
ndc (package): 84167-323-03
ndc (product): 84167-323
ndc11 (package): 84167032303
spl id: 48dd7f6e-2a4e-2c92-e063-6294a90a4255
spl set id: 48dd7f6e-2a4d-2c92-e063-6294a90a4255

Reported adverse events (FAERS/openFDA)#

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