KONEUK SUNSCREEN SPF50 cream

KONEUK SUNSCREEN SPF50 by

Drug Labeling and Warnings

KONEUK SUNSCREEN SPF50 by is a Otc medication manufactured, distributed, or labeled by Guangzhou Meixi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

HOMOSALATE,OCTOCRYLENE,AVOBENZONE,ENSULIZOLE,TITANIUM DIOXIDE

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children section

PURPOSE

Sunscreen

WARNINGS

keep out reach of children

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

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

INDICATIONS & USAGE

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KONEUK SUNSCREEN SPF50 
koneuk sunscreen spf50 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84167-323
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1 g
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	1 g

Inactive Ingredients
Ingredient Name	Strength
PROPANEDIOL (UNII: 5965N8W85T)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
GLYCERIN (UNII: PDC6A3C0OX)
2-BROMO-4'-HYDROXYACETOPHENONE (UNII: 6H0QU4I6BA)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
CITRIC ACID (UNII: 2968PHW8QP)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
FRAGRANCE 13576 (UNII: 5EM498GW35)
DIBUTYL ADIPATE (UNII: F4K100DXP3)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
PEG-100 STEARATE (UNII: YD01N1999R)
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
CALCIUM DISODIUM EDTA (UNII: 8U5D034955)
DISODIUM ALPHA-TOCOPHERYL PHOSPHATE, DL- (UNII: 35ZC9LRM4U)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALLANTOIN (UNII: 344S277G0Z)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
C14-22 ALCOHOLS (UNII: B1K89384RJ)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POLYSORBATE 60 (UNII: CAL22UVI4M)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84167-323-03	5 in 1 BOX	01/21/2026
1		1 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/21/2026

Labeler - Guangzhou Meixi Biotechnology Co., Ltd. (625724571)