COXIR CERAMIDE DAILY UV SUN BLOCK by NOKSIBCHO cosmetic Co., Ltd. Drug Facts

COXIR CERAMIDE DAILY UV SUN BLOCK by

Drug Labeling and Warnings

COXIR CERAMIDE DAILY UV SUN BLOCK by is a Otc medication manufactured, distributed, or labeled by NOKSIBCHO cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

COXIR CERAMIDE DAILY UV SUN BLOCK- titanium dioxide cream 
NOKSIBCHO cosmetic Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

titanium dioxide

Micro particle titanium dioxide
Aluminum hydroxide
Stearic acid
Cyclomethicone
PEG-10 Dimethicone
Isohexadecane
Micro particle zinc oxide
Methicone
Cyclomethicone
PEG-10 Dimethicone
Ethylhexyl Methoxycinnamate
Isoamyl p-Methoxycinnamate
Cyclopentasiloxane
4-Methylbenzylidene Camphor
PEG-10 Dimethicone
Glycerin
Cetyl PEG/PPG-10/1 Dimethicone
Disteardimonium Hectorite
Isononyl Isononanoate
Beeswax
Ozokerite
Sodium Hyaluronate
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
Collagen Extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Magnesium Sulfate
Hydrogenated Lecithin
Linoleic acid
Water
Glycerin
Ceramide NP
TEA-cocoyl Glutamate
Caprylic/capric Triglyceride
Camellia Japonica seed oil
Phenoxyethanol
Ethylhexylglycerin
Parfum

sun block

keep out of reach of the children

Can be used daily 15 minutes before sun exposure. Apply evenly to face and neck. Always reapply as needed.

For external use only
When using this product

■ if the following symptoms occurs after use, stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COXIR CERAMIDE DAILY UV SUN BLOCK 
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73590-0059
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4.95 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73590-0059-1	80 mL in 1 TUBE; Type 0: Not a Combination Product	09/07/2020	10/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	09/07/2020	10/07/2020

Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)

Establishment
Name	Address	ID/FEI	Business Operations
NOKSIBCHO cosmetic Co., Ltd.		690182175	manufacture(73590-0059)

Revised: 2/2023

Document Id: bf08c7c8-431e-4560-82bd-70ee58b7550b

34390-5

Set id: aecb2c70-1dd5-b671-e053-2a95a90a2a14

Version: 3

Effective Time: 20230227