Kandesn CC Cream

Manufacturer
Sunrider Manufacturing L.P.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:46:50

Label at a glance#

ProductKandesn CC Cream Light Medium
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Dosage and administration

DIRECTIONS: apply liberally 15 minutes before sun exposure Reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: limit time...

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

USES:

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreased the risk of skin cancer and early skin aging caused by the sun.

Directions

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:

  • apply liberally 15 minutes before sun exposure
  • Reapply:
  • after 40 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • Sun Protection Measures.
  • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
    • limit time in the sun, expecially from 10 a.m. - 2 p.m.
    • wear long-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Other information

  • protect this product from excessive heat and direct sun

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Titanium Dioxide 8.6%
Zinc Oxide 4.6%

INACTIVE INGREDIENT SECTION

OTHER INGREDIENTS:

Water (Deionized)
Caprylic/CapricTriglyceride,

Octyldodecyl Neopentanoate,

VP/Eicosene Copolymer,

Cyclopentasiloxane,

Glyceryl Stearate,
PEG-100 Stearate,

Squalane (Veg. Origin),

Cetyl Alcohol,
Dimethicone,

Alumina,
Olea Europaea (Olive) Fruit Oil,

Persea Gratissima (Avocado) Oil,

Simmondsia Chinensis (Jojoba) Seed Oil,

Tocopheryl Acetate (Natural),

Phenoxyethanol,

Glycerin,

Iron Oxides (CI 77491, 77492, 77499),

Magnesium Aluminum Silicate,

Polyhydroxystearic Acid,

Phenyl Trimethicone,

Citric Acid,

Hexyldecanol,

Ticaxan Xanthan Powder,

Cyclomethicone,

Propylene Glycol,

Trisodium EDTA,

Triethoxycaprylylsilane,

Ethylhexylglycerin,

Lysine PCA,

d-Tocopherol (Vitamin E),

Natural Scent Green Tea,

Cucumber Sage,

Sodium Benzoate Powder NF,

Ceramide-3,

Panicum Miliaceum (Millet) Seed Extract,

Cellulose Gum,

Melon Berry,

Phospholipids,

TEA-Carbomer,

Silica,

Avena Sativa (Oat) Kernel Protein,

Sodium Polyacrylate,

Ruscus Aculeatus Root Extract (Butcherbroom),

Symphytum Officinale Rhizome (Comfrey) Root Extract,

Hydrolyzed Wheat Protein,

Plantago Ovata (Plantain) Seed Extract,

Ceratonia Siliqua (Carob) Gum,

Potassium Sorbate,

Proline,

Serine,

Glutamine,

Leucine

WARNINGS SECTION

WARNINGS:

FOR EXTERNAL USE ONLY

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. If product is swallowed, get medical help or contact a Poison Control Center right away.

Box and Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBOXBOXTube lblTube lblTube

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
73df98bc-429f-4587-8299-6ad8d52a4f36Product name220250304
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
64b87b8d-6ae7-cef1-8fd2-34228b0cc1bcProduct name120140508

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62191-21362191-213-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 56 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5029be3c-9660-f152-e063-6294a90a77a69ccdccfe-c3ee-4e56-996f-6f7a1a8aa2572026-04-23WarningsExact identifier
spl set id: 9ccdccfe-c3ee-4e56-996f-6f7a1a8aa257

Reported adverse events (FAERS/openFDA)#

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