FDA.reportPublic FDA data

Calypso Magic Concealer Yellow Beige

Manufacturer
Aquacube Inc. | Caring Japan Inc.
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:26

Label at a glance#

ProductCalypso Magic Concealer Yellow Beige
Active ingredientTITANIUM DIOXIDE
Label structure6 sections

Dosage and administration

Apply liberally before sun exposure and as needed children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 8.36%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

Warnings When using this product

  • keep out of the eye area
  • rinse with water to remove
  • stop use and ask a doctor if rash or irritation develops
  • for external use onlyl
  • keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally before sun exposure and as needed
  • children under 6 months of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

water, cyclopentasiloxane, butylene glycol, triethylhexanoin, polymethylsilsesquioxane, dimethicone, cetyl PEG/PPG-10/1 dimethicone, sorbitol, PEG-10 dimethicone, sodium hyaluronate, royal jelly extract, aloe barbadensis leaf extract, hydroxypropyltrimonium hyaluronate, soluble collagen crosspolymer, hydrolyzed hyaluronic acid, hydrolyzed collagen, soluble collagen, dipotassium glycyrrhizate, trimethylsiloxysilicate, Limnanthes alba (meadowfoam) seed oil, squalene, polyglyceryl-2 diisostearate, magnesium sulfate, triethosycaprylylsilane, hydrogen dimethicone, methicone, alumina, calcium sodium borosilicate, nylon-12, silver oxide, disteardimonium hectorite, polysorbate 80, glycerin, sodium citrate, tocopherol, disodium EDTA, phenoxyethanol, aluminum hydroxide, synthetic fluorphlogopite, iron oxides, barium sulfate, talc

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79623-00379623-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
c576407d-3085-590d-e053-2995a90a5d0baa7d7b4d-3a60-1ace-e053-2a95a90ab0b82021-06-23WarningsExact identifier
spl set id: aa7d7b4d-3a60-1ace-e053-2a95a90ab0b8

Reported adverse events (FAERS/openFDA)#

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