MAY MORNING CUSHION 21

Manufacturer
In This Morning
Effective date
2017-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:15:27

Label at a glance#

ProductMAY MORNING CUSHION 21
Active ingredientDIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Dimethicone

INACTIVE INGREDIENT SECTION

Phenyl Trimethicone, Silica, Bis-Diglyceryl, Polyacyladipate-2, Octyldodecanol, Vinyl Dimethicone/Methicone, Silsesquioxane Crosspolymer, Isononyl Isononanoate, HDI/Trimethylol Hexyllactone Crosspolymer, Kaolin, Diisostearyl Malate, Titanium Dioxide (CI 77891), Silica Silylate, Polyglyceryl-2 Triisostearate, Dicalcium Phosphate, VP/Hexadecene Copolymer, Cetearyl Dimethicone/Vinyl Dimethicone Crosspolymer, IronOxides (CI77492), Sodium Hyaluronate, Glycerin, Microcrystalline Wax, Sorbitan Isostearate, Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, Polyglyceryl-2 Diisostearate, Tocopheryl Acetate, Water, Sodium PCA, Urea, Trehalose, Polyquaternium-51, Triacetin, Dehydroacetic Acid,Fragrance(Parfum), Iron Oxides (CI 77491), Red 7 (CI 15850:1), Yellow 5 Lake (CI 19140), Iron Oxides (CI 77499)

OTC - PURPOSE SECTION

helps skin whitening and wrinkle care
protects the skin from ultraviolet rays

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children


INDICATIONS & USAGE SECTION

apply proper amount 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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DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71217-001871217-0018-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OACTIB

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
9a7e495a-e131-1938-e053-2a95a90ab94652b170d3-92c8-55fc-e054-00144ff8d46c2019-12-24WarningsExact identifier
spl set id: 52b170d3-92c8-55fc-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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