PROTECTIVE BASE SUN FOR OILY SKIN

Manufacturer
In This Morning
Effective date
2017-02-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:19:47

Label at a glance#

ProductPROTECTIVE BASE SUN FOR OILY SKIN
Active ingredientNIACINAMIDE, ZINC OXIDE, TITANIUM DIOXIDE, ADENOSINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide, Titanium Dioxide, Niacinamide, Adenosine

INACTIVE INGREDIENT SECTION

Water, Cyclomethicone, Alcohol Denat., Ethylhexyl Methoxycinnamate, Cyclomethicone, Butylene Glycol, Glycerin, Dicaprylyl Carbonate, Silica, Octocrylene, Caprylyl Methicone, PEG-10 Dimethicone, Polymethyl Methacrylate, Methyl Methacrylate Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Enantia Chlorantha Bark Extract, Pinus Pumilio Bark Extract, Milk Lipids, Polymethylsilsesquioxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Aluminum Hydroxide, Glyceryl Caprylate, Stearic Acid, Disteardimonium Hectorite, Cetyl PEG/PPG-10/1 Dimethicone, Dimethicone/Methicone Copolymer, Caprylyl Glycol, Caprylic/ Capric Triglyceride, Dipropylene Glycol, Hydrogenated Phospatidylcholine, Theanine, Glutathione, Talc, Disodium EDTA, Phenoxyethanol

OTC - PURPOSE SECTION

Helps skin whitening and wrinkle care. Protects the skin from ultraviolet rays (SPF50+/PA+++).

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children


INDICATIONS & USAGE SECTION

After the basic skin care, shake well and evenly apply on to the skin.

WARNINGS SECTION

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71217-001171217-0011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
9a7d6fd7-bd53-11d7-e053-2995a90a8ec247ff52de-6166-349d-e054-00144ff88e882019-12-24WarningsExact identifier
spl set id: 47ff52de-6166-349d-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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