TIZO ULTRA NON TINTED MINERAL SUNSCREEN 3.5OZ (IS0385)

Manufacturer
Fallien Cosmeceuticals, LTD | Inspec Solutions LLC
Effective date
2026-05-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:59:06

Label at a glance#

ProductTIZO ULTRA NON TINTED MINERAL SUNSCREEN
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE
Label structure7 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

 ■ 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 risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures lncludlng: ■ limit time In the...

Label contents#

Full prescribing information#

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 useon damaged or broken skin.

When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Polson Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

 ■ 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 risk, regularly use a
sunscreen with broad spectrum SPF of 15 or higher and other sun
protection measures lncludlng: ■ limit time In the sun, especlally
from 10am to 2pm ■ wear long-sleeved shirts, pants, hats, and
sunglasses ■ children under 6 months: ask a doctor ■ do not spray
directly Into face. Spray on hands then apply to face ■ use In
well-ventilated area.

Other information

OTHER SAFETY INFORMATION

protect this product from excessive
heat and direct sun ■ may stain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane
Dimethicone Crosspolymer
Cyclopentasiloxane
Cyclohexasiloxane
Cyclopentasiloxane
Dimethiconol
Stearyl Dimethicone
Octadecene
Dimethicone
Polyglyceryl-4 Isostearate
Cetyl PEG/PPG-10/1 Dimethicone
PEG-30 Dipolyhydroxystearate
Tetrahexyldecyl Ascorbate
Tocopheryl Acetate
C12-15 Alkyl Benzoate
Microcrystalline Wax
Caprylhydroxamic Acid
Caprylyl Glycol
Glycerin

Disodium EDTA
Sodium Chloride
Polysorbate 20
Triethanolamine
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58892-072-04TIZO ULTRA NON TINTED MINERAL SUNSCREEN100 g in 1 TUBELOTION1002

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58892-07258892-072-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
TIZO ULTRA NON TINTED MINERAL SUNSCREENZINC OXIDE 20%Fallien Cosmeceuticals, LTD30d30610-2e6c-418c-bbcf-4ecd7f61be932026-05-28WarningsExact identifier
ndc (package): 58892-072-04
ndc (product): 58892-072
ndc11 (package): 58892007204
spl id: 52e1f59b-accd-1ee0-e063-6294a90a4a2d
spl set id: 30d30610-2e6c-418c-bbcf-4ecd7f61be93

Reported adverse events (FAERS/openFDA)#

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