FDA.reportPublic FDA data

Dr.Jucre Rebirth Sun Protection

Manufacturer
NATURECELL CO., LTD. | Cosmax, Inc.
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:50:25

Label at a glance#

ProductDr.Jucre Rebirth Sun Protection
Active ingredientOCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE
Label structure10 sections

Indications and uses

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

Dosage and administration

■ 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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Sunscreen
Skin Brightening
Anti wrinkle

WARNINGS

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Uses

INDICATIONS & USAGE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ 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

OTHER SAFETY INFORMATION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton ImageCarton Image

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ADENOSINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83071-150-01Dr.Jucre Rebirth Sun Protection65 mL in 1 CONTAINERCREAM651
83071-150-02Dr.Jucre Rebirth Sun Protection1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83071-150DR.JUCRE REBIRTH SUN PROTECTION (OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE) CREAM [NATURECELL CO., LTD.]1Current NDC, 2 package rows20250103_2ab49052-085f-024e-e063-6394a90a81b8.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83071-15083071-150-01, 83071-150-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIMETHICONE92RU3N3Y1OIACT
OCTINOXATE4Y5P7MUD51ACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
ENSULIZOLE9YQ9DI1W42ACTIB
OCTOCRYLENE5A68WGF6WMACTIB
BEMOTRIZINOLPWZ1720CBHACTIB
NIACINAMIDE25X51I8RD4ACTIB
ADENOSINEK72T3FS567ACTIB

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
Dr.Jucre Rebirth Sun ProtectionOCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINENATURECELL CO., LTD.2ab49052-085f-024e-e063-6394a90a81b82025-01-02WarningsExact identifier
ndc (package): 83071-150-02
ndc (package): 83071-150-01
ndc (product): 83071-150
ndc11 (package): 83071015001
ndc11 (package): 83071015002
spl id: 2ab47dd5-c8aa-0224-e063-6394a90acee4
spl set id: 2ab49052-085f-024e-e063-6394a90a81b8

Reported adverse events (FAERS/openFDA)#

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