Protecting may morning cushion 21 (refill)

Manufacturer
inthismorning co ltd | cosmax inc
Effective date
2023-01-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:53:36

Label at a glance#

ProductProtecting may morning cushion 21 (refill)
Active ingredientLINALOOL, (+/-)-, .BETA.-CITRONELLOL, (R)-, GERANIOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

citronellol, geraniol, linalool

INACTIVE INGREDIENT SECTION

Water
Phenyl Trimethicone
Ethylhexyl Methoxycinnamate
Cyclopentasiloxane
Titanium Dioxide (CI 77891)
Zinc Oxide (CI 77947)
Ethylhexyl Salicylate
Cetyl PEG/PPG-10/1 Dimethicone
Cyclohexasiloxane
Butylene Glycol
Butylene Glycol Dicaprylate/Dicaprate
Diisostearyl Malate
Glycerin
Niacinamide
Trimethylsiloxysilicate
1,2-Hexanediol
Acrylates/Stearyl Acrylate/Dimethicone Methacrylate Copolymer
Magnesium Sulfate
Mica (CI 77019)
Disteardimonium Hectorite
Sorbitan Isostearate
Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer
Aluminum Hydroxide
Iron Oxides (CI 77492)
Stearic Acid
Dimethicone/Vinyl Dimethicone Crosspolymer
Ethylhexylglycerin
Centella Asiatica Extract
Chamomilla Recutita (Matricaria) Flower Extract
Dimethicone
Glyceryl Caprylate
Triethoxycaprylylsilane
Iron Oxides (CI 77491)
Adenosine
Iron Oxides (CI 77499)
Disodium EDTA
Pelargonium Graveolens Flower Oil
Rose Flower Oil
Propanediol
Hyaluronic Acid
Hydrolyzed Hyaluronic Acid
Sodium Hyaluronate

OTC - PURPOSE SECTION

brightening, wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children

INDICATIONS & USAGE SECTION

push the puff gently into the cushion and apply it from larger areas to smaller areas

spread it evenly by lishtly patting onto the skin

WARNINGS SECTION

This product is for exeternal use only. Do not use for internal use
Storage and handling precautions
If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
Avoid placing the product near fire and store out in reach of children

- consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product

- do not use on wounded area

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GERANIOL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71217-0058-1Protecting may morning cushion 21 (refill)13 g in 1 POUCHPOWDER131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71217-0058PROTECTING MAY MORNING CUSHION 21 (REFILL) (CITRONELLOL, GERANIOL, LINALOOL) POWDER [INTHISMORNING CO LTD]1Current NDC, 1 package rows20230131_f384f8f2-9d5a-69f1-e053-2a95a90af6b9.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71217-005871217-0058-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Protecting may morning cushion 21 (refill)CITRONELLOL, GERANIOL, LINALOOLinthismorning co ltdf384f8f2-9d5a-69f1-e053-2a95a90af6b92023-01-30WarningsExact identifier
ndc (package): 71217-0058-1
ndc (product): 71217-0058
ndc11 (package): 71217005801
spl id: f384fa12-35eb-ac13-e053-2995a90ac33f
spl set id: f384f8f2-9d5a-69f1-e053-2a95a90af6b9

Reported adverse events (FAERS/openFDA)#

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