KISS MY FACE SUNSCREEN TATTOO SHADE BROAD SPECTRUM SPF 30- octinoxate, octisalate, zinc oxide cream

KISS MY FACE SUNSCREEN TATTOO SHADE broad spectrum spf 30 by

Drug Labeling and Warnings

KISS MY FACE SUNSCREEN TATTOO SHADE broad spectrum spf 30 by is a Otc medication manufactured, distributed, or labeled by Kiss My Face LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Octinoxate 7.5%, Octisalate 4.5%, Zinc Oxide 3%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only

Do not use

on damaged/broken skin

Stop use/ask a doctor

if rash occurs

When using this product

keep out of eyes. Rinse with water to remove

Keep out of reach of children

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply liberally 15 minutes before sun exposure Reapply after 40 minutes swimming/sweating immediately after towel drying atleast every 2 hours Children under 6 months: Ask a doctor Sun Protection Measures Spending time in the sun increases your risk of skin cancer/skin aging. To decrease risk, use Broad Spectrum sunscreen SPF 15 or higher and other protection measures including Limit time in sun, especially from 10am-2pm Wear long-sleeved shirts, pants, hats and sunglasses

Inactive Ingredients

Acrylates Copolymer, Avena Sativa (Oat) Beta-glucan, Avena Sativa (Oat) Protein, Camellia Sinensis (Green Tea) Leaf Extract, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Alcohol, Cetearyl Olivate, Cucumis Sativus (Cucumber) Extract, Daucus Carota Satova (Carrot) Root Extract, Ethylhexylglycerin, Glycerin, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Seed Oil, Phenoxyethanol, Polysorbate 20, Sorbitan Olivate, Stearic Acid, Water, Xanthan Gum

Other Information

Protect product from excessive heat and direct sun

Product Label

INGREDIENTS AND APPEARANCE

KISS MY FACE SUNSCREEN TATTOO SHADE BROAD SPECTRUM SPF 30 
octinoxate, octisalate, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65364-217
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	45 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CARROT (UNII: L56Z1JK48B)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SORBITAN OLIVATE (UNII: MDL271E3GR)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65364-217-88	1 in 1 CARTON	02/08/2017
1		88 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	01/09/2015

Labeler - Kiss My Face LLC (041794279)