Go Daily Defense Probiotic Mineral Face Moisturizer

Manufacturer
SOLARA SUNCARE, INC.
Effective date
2023-02-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:38:21

Label at a glance#

ProductGo Daily Defense Probiotic Mineral Face Moisturizer SPF-30
Active ingredientZINC OXIDE
Label structure10 sections

Indications and 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

Dosage and administration

shake or knead before each use apply generously and evenly to face and neck 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 the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and ...

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 19%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USES

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • shake or knead before each use
  • apply generously and evenly to face and neck 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 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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.

QUESTIONS OR COMMENTS

OTC - QUESTIONS SECTION

  • 1-855-859-1600 (9am – 5pm ET)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0-UC_Go_Daily Defense Probiotic Mineral Face Moisturizer_SPF-30_50mL0-UC_Go_Daily Defense Probiotic Mineral Face Moisturizer_SPF-30_50mL

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73054-11573054-115-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1fbe94d7-68f3-304f-e063-6294a90a4b26f3a87581-808d-609e-e053-2995a90ad8f42024-08-15WarningsExact identifier
spl set id: f3a87581-808d-609e-e053-2995a90ad8f4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.