CALIFORNIA ALOE POWER LASTING SUN BLOCK

Manufacturer: NATURE REPUBLIC CO., LTD. | Cosmax, Inc.
Effective date: 2019-12-31
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 23:47:32

Label at a glance#

ProductCALIFORNIA ALOE POWER LASTING SUN BLOCK

Active ingredientOCTINOXATE, Zinc Oxide, OCTISALATE, Titanium Dioxide

Label structure8 sections

Indications and uses

How to Use: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

Dosage and administration

How to Use: Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate 7.00%, Zinc Oxide 4.90%, Ethylhexyl Salicylate 4.50%, Titanium Dioxide 2.91%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Ingredients:
Water, Cyclopentasiloxane, Butylene Glycol, Glycerin, Cyclohexasiloxane, Caprylyl Methicone, PEG-10 Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Magnesium Sulfate, Disteardimonium Hectorite, Aloe Barbadensis Leaf Juice, Dimethicone/Vinyl Dimethicone Crosspolymer,
Aluminum Hydroxide, Stearic Acid, Phenoxyethanol, Caprylyl Glycol, Glyceryl Caprylate, Fragrance(Parfum), Dimethicone, Hibiscus Rosa-Sinensis Flower/Leaf Extract, Morinda Citrifolia Fruit Extract, Sea Water, Ethyl Hexanediol, Leuconostoc/Radish Root Ferment Filtrate,
Sodium Benzoate, Citric Acid, Pentylene Glycol, 1,2-Hexanediol

PURPOSE

OTC - PURPOSE SECTION

Purpose: UV Protection

WARNINGS

WARNINGS SECTION

Cautions:
For external use only.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use:
Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use:
Take an adequate amount of the product and thoroughly apply on the areas exposed to the UV rays.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51346-242-01	2021-07-13	C162847	48780-1	ba0f9c33-2b8a-a910-e053-dadaa90a0b85	79e6b838-0a88-4b4a-b9c3-93a87cef677b
51346-242-01	2021-01-29	C162847	48780-1	ba0f9c33-2b8a-a910-e053-dadaa90a0b85	79e6b838-0a88-4b4a-b9c3-93a87cef677b

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OCTISALATE	ACTIVE INGREDIENT	4X49Y0596W	1
Titanium Dioxide	ACTIVE INGREDIENT	15FIX9V2JP	1
Zinc Oxide	ACTIVE INGREDIENT	SOI2LOH54Z	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
OCTISALATE	ACTIVE MOIETY	4X49Y0596W	1
TITANIUM DIOXIDE	ACTIVE MOIETY	15FIX9V2JP	1
ZINC CATION	ACTIVE MOIETY	13S1S8SF37	1
Butylene Glycol	INACTIVE INGREDIENT	3XUS85K0RA	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

CALIFORNIA ALOE POWER LASTING SUN BLOCK
OCTINOXATE, Zinc Oxide, OCTISALATE, Titanium Dioxide
OCTINOXATE
Zinc Oxide
ZINC CATION
OCTISALATE
Titanium Dioxide
Water
Butylene Glycol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51346-242	51346-242-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
Zinc Oxide	SOI2LOH54Z	ACTIM
OCTISALATE	4X49Y0596W	ACTIB
Titanium Dioxide	15FIX9V2JP	ACTIB
Water	059QF0KO0R	IACT
Butylene Glycol	3XUS85K0RA	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Butylene Glycol	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TRANSDERMAL	8.12 mg		Exact identifier — unii candidate 2 equally ranked IID candidates
Butylene Glycol	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TOPICAL		1400 mg	Exact identifier — unii candidate 2 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
13e9d535-13ad-486f-ad53-25624160f949			79e6b838-0a88-4b4a-b9c3-93a87cef677b	2021-07-13	Warnings	Exact identifier spl set id: 79e6b838-0a88-4b4a-b9c3-93a87cef677b

Reported adverse events (FAERS/openFDA)#

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