KISS MY FACE SPF-50 Face Factor Mineral Sunscreen

Manufacturer
WINDMILL HEALTH PRODUCTS LLC
Effective date
2023-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:00:15

Label at a glance#

ProductKISS MY FACE SPF-50 Face Factor Mineral Sunscreen
Active ingredientZINC OXIDE
Label structure8 sections

Indications and uses

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

Dosage and administration

Apply liberally 15 minute before sun exposure. Reapply: after 80 minutes of swimming or sweating, immediately after towel drying and at least every 2 hours. Children under 6 months: ask a doctor. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use sunscreen with Broad Spectrum SPF 15 or higher and other sun protection measures including: Sun Protection ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide - 12.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

not intended for ingestion. 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 ask a doctor if

OTC - STOP USE SECTION

  • skin rash or irritation develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact Poison Control Center right away..

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • ask a health professional before use.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minute before sun exposure.
  • Reapply:
  • after 80 minutes of swimming or sweating,
  • immediately after towel drying and
  • at least every 2 hours.
  • Children under 6 months: ask a doctor.
  • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use sunscreen with Broad Spectrum SPF 15 or higher and other sun protection measures including: Sun Protection Measures:
  • Limit time in sun, especially from 10am to 2pm.
  • Wear long-sleeved shirts, pants, hats and sunglasses.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Acetyl Hexapeptide-8, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbic Acid (Vitamin C), Butylene Glycol, Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Carbomer. Cetearyl Alcohol, Chamomilla Recutita (Chamomile) Extract, Citrullus Lanatus (Watermelon) Extract, Cocos Nucifera (Coconut) Oil, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Citric Acid, Decyl Glucoside, Ethylhexylglycerin, Fucus Vesiculosus (Algae) Extract, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, Hydroxyethylcellulose, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Persea Gratissima (Avocado) Oil, Phenoxyethanol, Polyhydroxystearic Acid, Polysorbate-20, Saccharide Isomerate, Tagetes Erecta (Lutein) Extract, Tocopheryl Acetate (Vitamin E), Tridecyl Salicylate, Xanthan Gum

Other Information

SPL UNCLASSIFIED SECTION

  • Protect this product from excessive heat and direct sun.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74154-319-00KISS MY FACE SPF-50 Face Factor Mineral Sunscreen59 mL in 1 TUBECREAM592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74154-319KISS MY FACE SPF-50 FACE FACTOR MINERAL SUNSCREEN (ZINC OXIDE) CREAM [WINDMILL HEALTH PRODUCTS LLC]2Current NDC, Legacy NDC, 1 package rows20231112_edc2c1e7-e1a8-4b49-96df-8a94eb6a242a.zip

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74154-31974154-319-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KISS MY FACE SPF-50 Face Factor Mineral SunscreenZINC OXIDEWINDMILL HEALTH PRODUCTS LLCedc2c1e7-e1a8-4b49-96df-8a94eb6a242a2023-11-11WarningsExact identifier
ndc (package): 74154-319-00
ndc (product): 74154-319
ndc11 (package): 74154031900
spl id: 09e2089e-a71c-9d2f-e063-6394a90a2282
spl set id: edc2c1e7-e1a8-4b49-96df-8a94eb6a242a

Reported adverse events (FAERS/openFDA)#

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