Daily Care Sun

Manufacturer
MIGUHARA
Effective date
2016-02-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:06

Label at a glance#

ProductDaily Care Sun
Active ingredientOctinoxate, Titanium Dioxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Ethylhexyl Methoxycinnamate 5.00%, Titanium Dioxide 1.12%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Cetearyl Alcohol, Isododecane, Butylene Glycol, Benzophenone-4, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Propylene Glycol, Cyclopentasiloxane, Helianthus Annuus (sunflower) Seed Oil, Triethanolamine, Acrylates Copolymer, Nylon-12, Microcrystalline Wax, BeesWax, Cyclomethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetearyl Glucoside, Stearic Acid, Palmitic Acid, Dimethicone, Butyrospermum Parkii (Shea) Butter, Sodium Polyacrylate, Tocopheryl Acetate, PEG/PPG-19/19 Dimethicone, Hexyl Laurate, Dimethicone Copolyol, Fragrance, Methyl Paraben, Carbomer, Ethylhexyl Stearate, Alumina, PropylParaben, Sodium Laureth Sulfate, Disodium EDTA, Trideceth-6, Bifida Ferment Lysate, Glycerin, Portulaca Oleracea Extract, Tocopherol, Hydrolyzed Collagen

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

1. Stop usage immediately if any of the below symptoms occur. Continued use could aggravate symptoms, so it is advisable to consult with a dermatologist immediately. 1) Symptoms include but not limited to: red spots, swelling, itchiness. 2) When having the same symptoms as above due to direct sunlight. 2. Do not apply to areas affected by dermatitis, eczema or wounds. 3. Storage and handling: 1) Tightly close lid after each use. 2 Keep out of reach of children 3) Store in a cool dry area, away from sunlight 4) Its SPF and Ultraviolet rays were measured according to functional cosmetic regulation.

Usage

DESCRIPTION SECTION

Usage: Take an appropriate amount and gently apply it on the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70380-160-012020-01-31C16284748780-19d75b9d1-0e2b-f424-e053-dadaa90a57ce49f63197-b99e-4203-b7dd-8cb6360591a2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70380-160-01Daily Care Sun50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70380-160DAILY CARE SUN (OCTINOXATE, TITANIUM DIOXIDE) CREAM [MIGUHARA]1Legacy NDC, 1 package rows20160222_49f63197-b99e-4203-b7dd-8cb6360591a2.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70380-16070380-160-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
9882697b-8524-4c82-bfc7-563c9f2656a649f63197-b99e-4203-b7dd-8cb6360591a22016-02-22WarningsExact identifier
spl id: 9882697b-8524-4c82-bfc7-563c9f2656a6
spl set id: 49f63197-b99e-4203-b7dd-8cb6360591a2

Reported adverse events (FAERS/openFDA)#

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