Label: KISS MY FACE SPF-50 FACE FACTOR MINERAL SUNSCREEN- zinc oxide cream
- NDC Code(s): 74154-319-00
- Packager: WINDMILL HEALTH PRODUCTS LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Drug Facts
- Active Ingredient
- Uses:
- Warnings:
-
Directions:
- 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:
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
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
KISS MY FACE SPF-50 FACE FACTOR MINERAL SUNSCREEN
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74154-319 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 120 mg in 1 mL Inactive Ingredients Ingredient Name Strength ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGAN OIL (UNII: 4V59G5UW9X) ASCORBIC ACID (UNII: PQ6CK8PD0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SHEA BUTTER (UNII: K49155WL9Y) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CHAMOMILE (UNII: FGL3685T2X) WATERMELON (UNII: 231473QB6R) COCONUT OIL (UNII: Q9L0O73W7L) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) FUCUS VESICULOSUS (UNII: 535G2ABX9M) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYALURONIC ACID (UNII: S270N0TRQY) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) AVOCADO OIL (UNII: 6VNO72PFC1) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SACCHARIDE ISOMERATE (UNII: W8K377W98I) LUTEIN (UNII: X72A60C9MT) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74154-319-00 59 mL in 1 TUBE; Type 0: Not a Combination Product 02/14/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/14/2022 Labeler - WINDMILL HEALTH PRODUCTS LLC (831136267)