Dr.Jucre Rebirth Sun Protection

Product NDC
83071-150
11-digit product format
830710150
Labeler code
83071
Product ID
83071-150_2ab47dd5-c8aa-0224-e063-6394a90acee4
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE
Dosage form
CREAM
Route
TOPICAL
Labeler
NATURECELL CO., LTD.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2024-11-30
Substance
OCTINOXATE; HOMOSALATE; OCTISALATE; AVOBENZONE; ENSULIZOLE; OCTOCRYLENE; BEMOTRIZINOL; NIACINAMIDE; ADENOSINE
Active strength
7.3; 6; 4.5; 4; 3.5; 2; 1.5; 2; .04 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes
Adenosine Receptor Agonist [EPC], Adenosine Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Dr.Jucre Rebirth Sun Protection
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE7.3 g/100mL
HOMOSALATE6 g/100mL
OCTISALATE4.5 g/100mL
AVOBENZONE4 g/100mL
ENSULIZOLE3.5 g/100mL
OCTOCRYLENE2 g/100mL
BEMOTRIZINOL1.5 g/100mL
NIACINAMIDE2 g/100mL
ADENOSINE.04 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4Y5P7MUD51Internal UNII lookup
V06SV4M95SInternal UNII lookup
4X49Y0596WInternal UNII lookup
G63QQF2NOXInternal UNII lookup
9YQ9DI1W42Internal UNII lookup
5A68WGF6WMInternal UNII lookup
PWZ1720CBHInternal UNII lookup
25X51I8RD4Internal UNII lookup
K72T3FS567Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2ab49052-085f-024e-e063-6394a90a81b8Available on FDA.report

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

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 (product): 83071-150

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83071-150-018307101500165 mL in 1 CONTAINER65 mlHistorical
83071-150-02830710150021 CONTAINER in 1 CARTON (83071-150-02) / 65 mL in 1 CONTAINER (83071-150-01) 1 container2024-11-30NoNoCurrent