DAILY CARE SUN- octinoxate, titanium dioxide cream

Daily Care Sun by

Drug Labeling and Warnings

Daily Care Sun by is a Otc medication manufactured, distributed, or labeled by MIGUHARA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

INACTIVE INGREDIENT

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

Purpose: Sunscreen

WARNINGS

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

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAILY CARE SUN 
octinoxate, titanium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70380-160
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	Octinoxate	2.50 g  in 50 mL
Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	Titanium Dioxide	0.56 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isododecane (UNII: A8289P68Y2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70380-160-01	50 mL in 1 CARTON; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/02/2016

Labeler - MIGUHARA (689204213)

Registrant - MIGUHARA (689204213)

Establishment
Name	Address	ID/FEI	Business Operations
MIGUHARA		689204213	manufacture(70380-160)