Bion Pure Mineral Sunscreen

Manufacturer
CA Botana International INC
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:46:04

Label at a glance#

ProductBion Pure Mineral Sunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

Warning and Precautions

WARNINGS AND PRECAUTIONS 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. Keep out of reach of children. If product is swallowed, get medical help or contact poison control center right away

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Helps prevent sunburn.If used as directed with other sun protection measured decreases the risk of skin cancer and early skin aging caused by the sun. Apply liberally 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reaply at least every 2 hours. Children under 6 months: Ask a doctor. Sun protection measurments: Spending in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with broad spectrumSPF 15 or higher and other sun protection measures including: limit time in the sun, specially from 10:00 am to 2:00 pm Wear long sleeve shirts, pants, hats, and sun glasses. Protect this product from excessive heat and direct sun

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Avoid contact with eyes,Keep out of reach of children, Do not apply to open wounds Stop use and ask a doctor if condition worsens or symptons persist for more than seven days, discontinue use of the product

Purpose section

OTC - PURPOSE SECTION

Sunscreen, helps prevent sunburn

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 19%

Warning

WARNINGS SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact poison control center right away

Indication of usage

INDICATIONS & USAGE SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact poison control center right away

Inactive Inggredients

INACTIVE INGREDIENT SECTION

Hyaluronic Acid, Cetearyl Alcohol,Glycerin, Horse Chestnut, Vanilla Planifolia Fruit, Xanthan Gum, Hydrated Silica, Alkyl (C12-15) Benzoate, Phenoxyethanol, Triethoxycaprylylsilane, Potassium Sorbate, Beeswax, Ascorbyl Palmitate, Stearic Acid, Ceteareth-15, Macadamia Ternifolia Seed oil, Mica, Isomalt, Green tea leaf. Polyhidroxystearic acid stearate, Olea Europaea (Olive) leaf powder, Vitis Vinifera (Grape) seed oil, Ascorbic Acid, Propanediol, .Alpha.-Tocopherol Acetate, D, Ethylhexylglycerin, Lecithin, Soybean, Caprylic/Capric Triglyceride,Tocopherol, Aloe, Decyl Oleate, Ethylhexyl Palmitate, Water, Shea Butter, Rosmarinus Officinalis (Rosemary) Leaf powder, Panthenol, Phosphatidylcholine, Soybean, Citric Acid, Orange oil, Niacinamide, Stearyl Alcohol, Centella Asiatica, Coco-Caprilate/Caprate, Phytate Sodium.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pure Mineral Sunscreen Broad SpectruPure Mineral Sunscreen Broad Spectru

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

Products#

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

DailyMed product names page 1 of 2 · 49 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35192-05835192-058-14

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 46 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
4b33e740-0b26-639d-e063-6294a90a61643430f836-622f-10bb-e063-6394a90a9ae22026-02-19WarningsExact identifier
spl set id: 3430f836-622f-10bb-e063-6394a90a9ae2

Reported adverse events (FAERS/openFDA)#

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