DOTERRA SUN FACE DAILY MOISTURIZER- zinc oxide lotion

doTERRA sun Face Daily Moisturizer by

Drug Labeling and Warnings

doTERRA sun Face Daily Moisturizer by is a Otc medication manufactured, distributed, or labeled by doTERRA International, LLC, Bell International Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient Purpose
Zinc Oxide 13%.......................................... Sunscreen

Mineral Sunscreen Daily Moisturizer

This dermatologist-tested, mineral-based, broad-spectrum
sun protection moisturizer delivers exponential
benefits so your skin can look and act as young as
you feel. Formulated with non-nano zinc oxide,
doTERRA sun Face Mineral Sunscreen Daily Moisturizer
provides lightweight SPF 28 UVA/UVB defense
against the sun and blue light protection.
Rich in antioxidants, vitamin E, and nourishing
botanicals such as evodia, grapeseed oil, and CPTG®
essential oils, this lightweight, hydrating sunscreen
moisturizer is intended for everyday use.

INDICATIONS & USAGE

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

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

WHEN USING

For sunscreen use: apply liberally 15 minutes before
sun exposure apply to all skin exposed to the sun
use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
†Children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Inactive ingredients Water (Aqua), Caprylic/Capric
Triglyceride, Butyloctyl Salicylate, Propanediol, Vitis
vinifera (Grape) Seed Oil, Cetearyl Alcohol, Cetyl
Alcohol, Evodia rutaecarpa (Evodia) Fruit Extract,
Persea gratissima (Avocado) Oil, Daucus carota sativa
(Carrot) Seed Oil, Boswellia carterii (Frankincense) Oil,
Helichrysum italicum Flower/Leaf/Stem Oil,
Astrocaryum tucuma Seed Butter, Rubus idaeus
(Raspberry) Seed Oil, Sodium Stearoyl Glutamate,
Arachidyl Alcohol, Caprylyl Glycol, Coco-Glucoside,
Xanthan Gum, Helianthus annuus (Sunflower) Seed Oil,
Cocos nucifera (Coconut) Fruit Extract, Michelia alba
(Magnolia) Leaf Oil, Cymbopogon flexuosus
(Lemongrass) Oil, Cananga odorata (Ylang Ylang)
Flower Oil, Aloe barbadensis Leaf Juice, Michelia alba
(Magnolia) Flower Oil, Ethyl Ferulate, Behenyl Alcohol,
Arachidyl Glucoside, Citric Acid, Sodium Gluconate,
Bisabolol, Caprylhydroxamic Acid, Tocopherol,
Polyhydroxystearic Acid, Phytosterols, Squalene, Citrus
nobilis (Mandarin Orange) Peel Oil

STORAGE AND HANDLING

Other information protect this product from
excessive heat and direct sun.

QUESTIONS

Questions or comments? Call 1-800-411-8151

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

DOSAGE & ADMINISTRATION

Apply topically

doTERRA sun Face Mineral Sunscreen Daily Moisturizer

Primary Label and Packaging

INGREDIENTS AND APPEARANCE

DOTERRA SUN FACE DAILY MOISTURIZER 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71630-147
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)
CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
CITRUS NOBILIS WHOLE (UNII: U29I7N5FLM)
CYMBOPOGON FLEXUOSUS WHOLE (UNII: 0MK18YOA5G)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EVODIA RUTAECARPA FRUIT, IMMATURE (UNII: F7M0RB6Y4I)
MICHELIA ALBA LEAF OIL (UNII: 002RK9L1FN)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
PROPANEDIOL (UNII: 5965N8W85T)
BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
ETHYL FERULATE (UNII: 5B8915UELW)
SUNFLOWER OIL (UNII: 3W1JG795YI)
GLUCOSE PENTAACETATE (UNII: 3040885R4N)
RASPBERRY SEED OIL (UNII: 9S8867952A)
DODECANEDIOIC ACID (UNII: 978YU42Q6I)
SODIUM GLUCONATE (UNII: R6Q3791S76)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
CARROT SEED OIL (UNII: 595AO13F11)
COCOS NUCIFERA WHOLE (UNII: 245J88W96L)
MICHELIA ALBA WHOLE (UNII: TKZ4AVY41O)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
GRAPE SEED OIL (UNII: 930MLC8XGG)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
COCO GLUCOSIDE (UNII: ICS790225B)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
BUTYLOCTANOL (UNII: N442D9VO79)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CETYL ALCOHOL (UNII: 936JST6JCN)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
TOCOPHEROL (UNII: R0ZB2556P8)
SQUALENE (UNII: 7QWM220FJH)
WATER (UNII: 059QF0KO0R)
AVOCADO OIL (UNII: 6VNO72PFC1)
HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71630-147-15	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/01/2023

Labeler - doTERRA International, LLC (832274935)

Establishment
Name	Address	ID/FEI	Business Operations
Bell International Laboratories		967781555	manufacture(71630-147)