NO SUN FACE SPF 50

Manufacturer
Naos USA, Inc.
Effective date
2022-01-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:04

Label at a glance#

ProductNO SUN FACE SPF 50
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

Help prevent sunburn.

Dosage and administration

Adults 18 years and older: • Apply liberally and evenly 15 minutes before sun exposure. • Reapply at least every 2 hours. • 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measu...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 19.9%

Titanium Dioxide 9%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Help prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs

Keep out reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control centre or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults 18 years and older:
    • Apply liberally and evenly 15 minutes before sun exposure.
    • Reapply at least every 2 hours.
    • 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 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. ; and
    • Wear long-sleeve shirts, pants, hats and sunglasses.
    • Children under 6 months of age: ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Keep the product between 15-30ºC (59-86ºF).
  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Aqua/Water, Cyclohexasiloxane, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Butylene Glycol, Dimethicone, Ethylhexyl Palmitate, Aluminum Hydroxide, Stearic Acid, Peg/Ppg-18/18 Dimethicone, Tocopheryl Acetate Sodium Chloride, Triethoxycaprylylsilane, Creatine, Glycyrrhetinic Acid, Mannitol, Pentylene Glycol, Sodium Dextran Sulfate, Hydrolyzed Soy Protein, Hydrolyzed Wheat Protein, Phenoxyethanol, Propylene Glycol, Caprylyl Glycol, Artemia Extract, Xanthan Gum, Carnosine, Disodium Adenosine Triphosphate, Tocopherol, Laminaria Digitata Extract, Potassium Sorbate. [Es873]

Questions?

OTC - QUESTIONS SECTION

Call 1-877-443-3762

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Label3Outer Label3Inner Label3Inner Label3

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14324-01214324-012-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
ea2f5066-653d-395b-e053-2995a90aa3fb64434256-5f5e-3a23-e053-2991aa0afee22022-10-04WarningsExact identifier
spl set id: 64434256-5f5e-3a23-e053-2991aa0afee2

Reported adverse events (FAERS/openFDA)#

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