DAILY DEFENSE MINERAL SUNSCREEN SERUM BROAD SPECTRUM SPF 33- zinc oxide lotion

Daily Defense Mineral Sunscreen Serum Broad Spectrum SPF 33 by

Drug Labeling and Warnings

Daily Defense Mineral Sunscreen Serum Broad Spectrum SPF 33 by is a Otc medication manufactured, distributed, or labeled by Eva's Esthetics, Sun Deep, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS

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

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 PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

• APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
• REAPPLY: AFTER 40 MINUTES OF SWIMMING OR SWEATING // IMMEDIATELY AFTER TOWEL DRYING // AT LEAST EVERY 2 HOURS
• 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 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-SLEEVE SHIRTS, PANTS, HATS, AND SUNGLASSES
• CHILDREN UNDER 6 MONTHS: ASK A DOCTOR

OTHER INFORMATION

• PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUN

QUESTIONS OR COMMENTS?

CALL TOLL FREE 1-800-765-7597

ACTIVE INGREDIENTS

17% ZINC OXIDE

PURPOSE

SUNSCREEN

INACTIVE INGREDIENTS

WATER (AQUA), PROPANEDIOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, DIMETHICONE, POLYGLYCERYL-6 POLYRICINOLEATE, C12-15 ALKYL BENZOATE, ISODODECANE, POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE, SQUALANE, POLYGLYCERYL-10 DIOLEATE, HYDROGENATED PHOSPHATIDYLCHOLINE, DISTEARDIMONIUM HECTORITE, MALUS DOMESTICA FRUIT CELL CULTURE EXTRACT, HYDROLYZED HYALURONIC ACID, TOCOPHERYL ACETATE, GLYCERIN, OCIMUM SANCTUM LEAF EXTRACT, WITHANIA SOMNIFERA ROOT EXTRACT, BISABOLOL, BUTYROSPERMUM PARKII (SHEA) BUTTER, CITRUS LIMON (LEMON) PEEL OIL , CITRUS TANGERINA (TANGERINE) PEEL OIL, CYMBOPOGON CITRATUS LEAF/STEM OIL, PROPYLENE CARBONATE, FRAGRANCE, BENZYL ALCOHOL, SODIUM CHLORIDE, SALICYLIC ACID, POLYSILICONE-11, SORBIC ACID, POLYHYDROXYSTEARIC ACID, DECYL GLUCOSIDE, ISOMALT

PRINCIPAL DISPLAY PANEL - 15 ml Bottle Carton

DAILY
DEFENSE

MINERAL
SUNSCREEN
SERUM

BROAD SPECTRUM
SPF 33

APPLE STEM CELL

HYALURONIC ACID

SQUALANE

T U E L
15 ml / 0.5 fl oz

INGREDIENTS AND APPEARANCE

DAILY DEFENSE MINERAL SUNSCREEN SERUM BROAD SPECTRUM SPF 33 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87432-704
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	0.17 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ISODODECANE (UNII: A8289P68Y2)
POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE (UNII: X2PZH4Y6HT)
SQUALANE (UNII: GW89575KF9)
POLYGLYCERYL-10 DIOLEATE (UNII: 598RES7AXX)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
HOLY BASIL LEAF (UNII: SCJ765569P)
WITHANIA SOMNIFERA ROOT (UNII: V038D626IF)
LEVOMENOL (UNII: 24WE03BX2T)
SHEA BUTTER (UNII: K49155WL9Y)
LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)
MANDARIN OIL (UNII: NJO720F72R)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SALICYLIC ACID (UNII: O414PZ4LPZ)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
SORBIC ACID (UNII: X045WJ989B)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ISOMALT (UNII: S870P55O2W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87432-704-01	1 in 1 CARTON	09/15/2023
1		15 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2	NDC: 87432-704-02	1 in 1 CARTON	09/15/2023
2		30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
3	NDC: 87432-704-03	1 in 1 CARTON	09/15/2023
3		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M020	09/15/2023

Labeler - Eva's Esthetics (051696292)

Establishment
Name	Address	ID/FEI	Business Operations
Sun Deep, Inc.		189788201	MANUFACTURE(87432-704)