Mineral Prismatic Luminizing Shield SPF 35

Manufacturer
Volition Beauty
Effective date
2023-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:30

Label at a glance#

ProductMineral Prismatic Luminizing Shield SPF 35
Active ingredientZinc Oxide
Label structure9 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 well. Apply over entire face 30 minutes before sun exposure. Reapply at least every 2 hours or as needed. Can be worn alone or under makeup. Use a water-resistant sunscreen if swimming or sweating. 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 Broad Spectrum SPF value of 15 or higher and other s...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 23.3%

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

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product avoid direct contact with eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop using and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Shake well. Apply over entire face 30 minutes before sun exposure.
  • Reapply at least every 2 hours or as needed. Can be worn alone or under makeup.
  • Use a water-resistant sunscreen if swimming or sweating.
  • 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. -1 p.m.
  • wear long-sleeve shirts, pants, hats and sunglasses
  • children under 6 months of age: Ask a doctor.

Other information

OTHER SAFETY INFORMATION

  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Ethylhexyl Olivate, C13-15 Alkane, Butyloctyl Salicylate, Polyglyceryl-3 Polyricinoleate, Sorbitan Isostearate, Argania Spinosa Kernel Oil, Tocopheryl Acetate, Triethoxycaprylylsilane, Synthetic Fluorphlogopite, Glycerin, Sodium Chloride, Squalane, Butylene Glycol, Actinidia Chinensis (Kiwi) Fruit Water, Sodium Benzoate, Bisabolol, Potassium Sorbate, Alcohol, Sophora Flavescens Root Extract, Hydrolyzed Sodium Hyaluronate, Glycyrrhiza Glabra (Licorice) Root Extract, Ascorbic Acid, Sodium Ferrocyanide, Hydrogenated Lecithin, Iron Oxides (Cl 77499), Iron Oxides (Cl 77492), Iron Oxides (Cl 77491), Titanium Dioxide (Cl 77891).

Principal Display Panel - 30 mL Carton Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VOLITION

MINERAL
PRISMATIC
LUMINIZING
SHIELD

SPF 35

30 ML / 1 FL OZ

Principal Display Panel - 30 mL Carton Label
Principal Display Panel - 30 mL Carton Label

Principal Display Panel - 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VOLITION

MINERAL
PRISMATIC
LUMINIZING
SHIELD

SPF 35

30 ML / 1 FL OZ

Principal Display Panel - 30 mL Bottle Label
Principal Display Panel - 30 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72577-525-122023-11-30C16284748780-1f386c649-9c10-0266-e053-dadaa90a7c1aDrug Facts
72577-525-122023-01-30C16284748780-1f386c649-9c10-0266-e053-dadaa90a7c1aDrug Facts

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72577-52572577-525-10, 72577-525-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
1d658b8a-5d05-4082-998e-559a0c95c12a420c9bc3-4935-42d5-bf28-55a8329b01862023-11-30WarningsExact identifier
spl id: 1d658b8a-5d05-4082-998e-559a0c95c12a
spl set id: 420c9bc3-4935-42d5-bf28-55a8329b0186

Reported adverse events (FAERS/openFDA)#

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