Cay Skin Universal Mineral Body Lotion SPF 55

Manufacturer
Cay Skin, Inc.
Effective date
2022-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:04:49

Label at a glance#

ProductCay Skin Universal Mineral Body SPF 55
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

Helps prevent sunburn If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

Adults and children over 6 months of age: Apply liberally 15 minutes before sun exposure. Reapply: at least every 2 hours or after 80 minutes of swimming, sweating or immediately after towel drying. Children under 6 months of age: ask a doctor. 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 Spe...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 10%

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and consult a doctor

OTC - STOP USE SECTION

if skin rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 6 months of age:

  • Apply liberally 15 minutes before sun exposure.
  • Reapply: at least every 2 hours or after 80 minutes of swimming, sweating or immediately after towel drying.
  • Children under 6 months of age: ask a doctor.
  • 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 value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m.; wear long-sleeved shirts, pants, hats and sunglasses.

Other information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Propanediol, Tridecyl Salicylate, Coco-Caprylate, Simmondsia Chinensis (Jojoba) Seed Oil, Isopropyl Isostearate, Squalane, Polyester-7, Cyclodextrin, Glyceryl Stearate, Neopentyl Glycol Diheptanoate, Polyglyceryl-3 Polyricinoleate, Sodium Chloride, Siica Silylate, Siica, Polyglyceryl-2 Dpolyhydroxystearate, Glycerin, Glyceryl Dibehenate, Bisabolol, Phenylpropanol, Allantoin, Rutin, Tribehenin, Caprylyl Glycol, Lecithin, Glyceryl Behenate, Citrullus Lanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Aloe Barbadensis Leaf Juice Powder, Maltodextrin, Sodium Lactate, Sodium Hyaluronate, Chondrus Crispus Extract, Vrtis Vinifera (Grape) Seed Extract, Iron Oxides, Sodium PCA, Potassium Sorbate, Sodium Benzoate, Tocopherol, Camellia Sinensis Leaf Extract, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Hydrogenated Lecithin

Questions or comments?

OTC - QUESTIONS SECTION

cayskin.com (256) 396-8268

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

universal bodyuniversal body

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82657-00482657-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 45 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
2889e778-60c4-16d6-e063-6394a90a02fcd929a719-5376-0c59-e053-2995a90aeec62024-12-05WarningsExact identifier
spl set id: d929a719-5376-0c59-e053-2995a90aeec6

Reported adverse events (FAERS/openFDA)#

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