GO DAILY DEFENSE SOOTHING MINERAL FACE SUNSCREEN SPF-30- zinc oxide lotion

Go Daily Defense Soothing Mineral Face Sunscreen by

Drug Labeling and Warnings

Go Daily Defense Soothing Mineral Face Sunscreen by is a Otc medication manufactured, distributed, or labeled by SOLARA SUNCARE, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Zinc Oxide 19%

PURPOSE

Sunscreen

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

Keep out of reach of children. If product is swallowed, get medical help or contact Poison Control Center right away.

DIRECTIONS

• shake before each use
• apply generously and evenly to face and neck 15 minutes before sun exposure
• use a water resistant sunscreen if swimming or sweating
• reapply 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 the 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-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor

INACTIVE INGREDIENTS

Water (Aqua), Caprylic/Capric Triglyceride, Coconut Alkanes, Cetearyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Coco-Glucoside, Lactobacillus Ferment, Camellia Sinensis (Green Tea) Leaf Extract, Helianthus Annuus (Sunflower) Sprout Extract, Hydrolyzed Jojoba Esters, Butyrospermum Parkii Nut Extract, Caesalpinia Spinosa Fruit Pod Extract, Caprylhydroxamic Acid, Glyceryl Caprylate, Cetearyl Glucoside, Caprylyl/Capryl Glucoside, Coco-Caprylate/Caprate, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin, Dipotassium Glycyrrhizinate, Sodium Phytate, Propylene Glycol, Xanthan Gum, Sclerotium Gum, Phenoxyethanol, Sodium Benzoate, Tocopherol

OTHER INFORMATION

• Protect this product from excessive heat and direct sun.

QUESTIONS OR COMMENTS

• 1-855-859-1600 (9am – 5pm ET)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GO DAILY DEFENSE SOOTHING MINERAL FACE SUNSCREEN   SPF-30
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73054-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	19 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
COCONUT ALKANES (UNII: 1E5KJY107T)
HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
ISOSTEARIC ACID (UNII: X33R8U0062)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
CAESALPINIA SPINOSA FRUIT POD (UNII: EXY4496LWD)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PHYTATE SODIUM (UNII: 88496G1ERL)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
TOCOPHEROL (UNII: R0ZB2556P8)
COCO GLUCOSIDE (UNII: ICS790225B)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
XANTHAN GUM (UNII: TTV12P4NEE)
SHEANUT (UNII: 84H6HBP32L)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73054-116-11	1 in 1 BOX	10/17/2021
1		50 mL in 1 BOTTLE; 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	10/17/2021

Labeler - SOLARA SUNCARE, INC. (040998319)