UV PROTECTION SUN BLOCK SPF50 PA by NOKSIBCHO cosmetic Co., Ltd. Drug Facts

UV PROTECTION SUN BLOCK SPF50 PA by

Drug Labeling and Warnings

UV PROTECTION SUN BLOCK SPF50 PA by is a Otc medication manufactured, distributed, or labeled by NOKSIBCHO cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UV PROTECTION SUN BLOCK SPF50 PA- 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

Water
Aluminum hydroxide
Stearic acid
Cyclomethicone
PEG-10 Dimethicone
Isohexadecane
Micro particle zinc oxide
Methicone
Cyclomethicone
PEG-10 Dimethicone
Ethylhexyl Methoxycinnamate
Dimethicone
Dimethicone/Vinyl Dimethicone Crosspolymer
Isoamyl p-Methoxycinnamate
Cyclopentasiloxane
Malva Sylvestris (Mallow) Flower Extract
4-Methylbenzylidene Camphor
PEG-10 Dimethicone
Sorbitan Sesquioleate
Cetyl PEG/PPG-10/1 Dimethicone
Isononyl Isononanoate
Disteardimonium Hectorite
Beeswax
Ozokerite
Butylene glycol
Sodium Hyaluronate
Leontopodium alpinum extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Magnesium Sulfate
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
Phenoxyethanol
Ethylhexylglycerin
Parfum

sun block

keep out of reach of the children

1. After smoothing your skin tone with your regular skin care products, apply a small amount of UV Protection Sun Block to your face.
2. Spread it softly on your whole face.
3. It makes your skin tone moist and clean

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

UV PROTECTION SUN BLOCK SPF50 PA 
titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73590-0055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE (UNII: NMQ347994Z)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73590-0055-2	50 mL in 1 TUBE; Type 0: Not a Combination Product	09/07/2020	09/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	09/07/2020	09/08/2020

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(73590-0055)

Revised: 9/2020

Document Id: aecb3934-2ec4-3a96-e053-2a95a90a7767

34390-5

Set id: aeb392ea-bb05-7bf7-e053-2a95a90aeaf9

Version: 4

Effective Time: 20200908