FDA.reportPublic FDA data

CLEMATIS Morning dew BB 21 Light Beige

Manufacturer
Coshub Co., Ltd. | COSON Co., Ltd._Osan Plant
Effective date
2017-09-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:25

Label at a glance#

ProductCLEMATIS Morning dew BB 21 Light Beige
Active ingredientTitanium Dioxide, Octinoxate, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 8.12%, Ethylhexyl Methoxycinnamate 7.00%, Zinc Oxide 4.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Cyclopentasiloxane, Phenyl Trimethicone, Cyclohexasiloxane, Dimethicone, Butylene Glycol, Butylene Glycol Dicaprylate/Dicaprate, PEG-10 Dimethicone, Glycerin, Niacinamide, Dicaprylyl Carbonate, Methyl Methacrylate Crosspolymer, Sodium Chloride, Disteardimonium Hectorite, Ozokerite, Trimethylsiloxyphenyl Dimethicone, Hydrogenated Polydecene, Hydrogenated Polyisobutene, Iron Oxides(CI77492), Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl Peg/Ppg-10/1 Dimethicone, Sorbitan Sesquioleate, Phenoxyethanol, Triethoxycaprylylsilane, Iron Oxides(CI77491), Beeswax, Iron Oxides(CI77499), Aluminum Hydroxide, Ethylhexylglycerin, Fragrance, Adenosine, Silica dimethyl silylate, Disodium EDTA

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: For external use only. Avoid contact with eyes. Replace the cap after use. 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: Apply the sun gel liberally to cover all parts of your face and body exposed to the sun's rays.

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
71702-090-022021-01-29C16284748780-1ba0f9c33-3705-a910-e053-dadaa90a0b85d4563e37-8cfa-4e77-83da-64118f9912c0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71702-090-01CLEMATIS Morning dew BB 21 Light Beige50 mL in 1 TUBECREAM501
71702-090-02CLEMATIS Morning dew BB 21 Light Beige1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71702-090CLEMATIS MORNING DEW BB 21 LIGHT BEIGE (TITANIUM DIOXIDE) CREAM [COSHUB CO., LTD.]1Legacy NDC, 2 package rows20170905_d4563e37-8cfa-4e77-83da-64118f9912c0.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
71702-09071702-090-01, 71702-090-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Titanium Dioxide15FIX9V2JPACTIB
Octinoxate4Y5P7MUD51ACTIB
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
e3f5ad72-c2d3-4b7c-975d-3b2047b9a6cdd4563e37-8cfa-4e77-83da-64118f9912c02017-09-05WarningsExact identifier
spl id: e3f5ad72-c2d3-4b7c-975d-3b2047b9a6cd
spl set id: d4563e37-8cfa-4e77-83da-64118f9912c0

Reported adverse events (FAERS/openFDA)#

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