FDA.reportPublic FDA data

CLEMATIS BASE CUSHION

Manufacturer
Coshub Co., Ltd. | EYESOME. Co.,Ltd.
Effective date
2017-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:24

Label at a glance#

ProductCLEMATIS BASE CUSHION
Active ingredientOctinoxate, Titanium Dioxide, Octisalate, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethylhexyl Methoxycinnamate 7.50%, Titanium Dioxide 6.05%, Ethylhexyl Salicylate 5.00%, Zinc Oxide 1.96%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Cyclopentasiloxane, Phenyl Trimethicone, Cyclohexasiloxane, Butylene Glycol, Glycerin, Niacinamide, Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone,PEG-10 Dimethicone, Aluminum Hydroxide, Magnesium Sulfate, Stearic Acid, Disteardimonium Hectorite, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Acrylates/Ethylhexyl Acrylate/Dimethicone Methacrylate Copolymer, Polyhydroxystearic Acid , Caprylyl Glycol, Methyl Methacrylate Crosspolymer, Allantoin, Tocopheryl Acetate, Lecithin, Ethylhexyl Palmitate, Isostearic Acid, Isopropyl Myristate, Iron Oxides (CI 77491), Caprylhydroxamic Acid, Triethoxycaprylylsilane, Adenosine, Polyglyceryl-3 Polyricinoleate, Disodium EDTA, Aloe Barbadensis Leaf Juice Powder, Biosaccharide Gum-1, Sophora Japonica Fruit Extract, Pancratium Maritimum Extract, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children.

DESCRIPTION

DESCRIPTION SECTION

Uses: - Helps prevent sunburn. - If used as directed with other sun protection measures (See Directions), decrease the risk of skin cancer and early skin aging caused by the sun

Directions: Gently press the pull on the air cushion and pat it onto your skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71702-010-022021-07-23C16284748780-1c7ccaba7-1d01-fd44-e053-dadaa90aa01b686d0611-18e8-4905-a42b-4887127a5091

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71702-010-01CLEMATIS BASE CUSHION13 g in 1 CONTAINERPOWDER131
71702-010-02CLEMATIS BASE CUSHION1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71702-010CLEMATIS BASE CUSHION (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE) POWDER [COSHUB CO., LTD.]1Legacy NDC, 2 package rows20170904_686d0611-18e8-4905-a42b-4887127a5091.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71702-01071702-010-01, 71702-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Octinoxate4Y5P7MUD51ACTIB
Titanium Dioxide15FIX9V2JPACTIB
Octisalate4X49Y0596WACTIB
Zinc OxideSOI2LOH54ZACTIM
Water059QF0KO0RIACT
Phenyl TrimethiconeDR0K5NOJ4RIACT

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
135597f2-0b90-45af-9a4a-fee4d371837c686d0611-18e8-4905-a42b-4887127a50912017-09-04WarningsExact identifier
spl id: 135597f2-0b90-45af-9a4a-fee4d371837c
spl set id: 686d0611-18e8-4905-a42b-4887127a5091

Reported adverse events (FAERS/openFDA)#

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