DR.JUCRE REBIRTH WHITE SUN PROTECTION- octinoxate, homosalate, octisalate, avobenzone, ensulizole, octocrylene, bemotrizinol, niacinamide, adenosine cream

Dr.Jucre Rebirth White Sun Protection by

Drug Labeling and Warnings

Dr.Jucre Rebirth White Sun Protection by is a Otc medication manufactured, distributed, or labeled by NATURECELL CO., LTD., Cosmax, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Ethylhexyl Methoxycinnamate 7.30%
Homosalate 6.00%
Ethylhexyl Salicylate 4.50%
Butyl Methoxydibenzoylmethane 4.00%
Phenylbenzimidazole Sulfonic Acid 3.50%
Octocrylene 2.00%
Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine 1.50%
Niacinamide 2.0%
Adenosine 0.04%

INACTIVE INGREDIENTS

Water, Butylene Glycol, Dimethicone, Dipropylene Glycol, Hydrogenated Poly(C6-14 Olefin), Neopentyl Glycol Diheptanoate, Cyclopentasiloxane, Methyl Methacrylate Crosspolymer, Aminomethyl Propanol, Cyclohexasiloxane, Caprylyl Methicone, Human Adipose Derived Stem Cell Conditioned Media, Potassium Cetyl Phosphate, Triceteareth-4 Phosphate, Glycol Stearate, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Silica, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, PEG-2 Stearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Glyceryl Caprylate, Santalum Album (Sandalwood) Oil, Caprylyl Glycol, Xanthan Gum, Polysorbate 60, Sorbitan Isostearate, Disodium EDTA, Hydroxypropyl Cyclodextrin, Plankton Extract, Thioctic Acid, 1,2-Hexanediol, Tremella Fuciformis (Mushroom) Extract, Potassium Hydroxide

PURPOSE

Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Skin Brightening
Anti wrinkle

WARNINGS

For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Replace the cap after use.
Refrain from using it on wounded areas.
Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

Uses

■ Helps prevent sun burn
■ Helps brighten skin tone
■ Helps improve wrinkle problem

Directions

■ Apply an appropriate amount evenly on the skin.
■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure. Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

Other Information

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light.

Questions

■ www.ibiostar.com
■ Tel (424)227-9568

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.JUCRE REBIRTH WHITE SUN PROTECTION 
octinoxate, homosalate, octisalate, avobenzone, ensulizole, octocrylene, bemotrizinol, niacinamide, adenosine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83071-060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.30 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6.00 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.50 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	4.00 g  in 100 mL
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	3.50 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.00 g  in 100 mL
BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH)	BEMOTRIZINOL	1.50 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2.00 g  in 100 mL
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Butylene Glycol (UNII: 3XUS85K0RA)
Dimethicone (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83071-060-02	1 in 1 CARTON	10/01/2022
1	NDC: 83071-060-01	65 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/01/2022

Labeler - NATURECELL CO., LTD. (689282572)

Registrant - NATURECELL CO., LTD. (689282572)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(83071-060)