Pollen UV Perfect Daily Sunscreen

Manufacturer
NSB Co., Ltd.
Effective date
2019-01-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:58:05

Label at a glance#

ProductPollen UV Perfect Daily Sunscreen
Active ingredientOCTINOXATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

• Apply liberally 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...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate (Ethylhexyl Methoxycinnamate) (7%)

Octisalate (Ethylhexyl Salicylate) (5%)

Octocyrlene (3%)

Titanium Dioxide (2%)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not swallow. In case of accidental ingestion, seek professional assistance

Warnings

WARNINGS SECTION

For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product
 Do not apply on other parts of the body
 Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
 Do not apply directly to wound or open cut.
Stop use and ask doctor if rash or irritation on skin develops and lasts.

Store at room temperature

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally 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.
 Wear long-sleeved shirts, pants, hats, and sunglasses.
Children under 6 months of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propanediol, Panthenol, Niacinamide, Phenylbenzimidazole Sulfonic Acid, 1,2-Hexanediol, Tromethamine, C14-22 Alcohols, Hydrogenated C6-14 Olefin Polymers, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Cetearyl Alcohol, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Glyceryl Stearate, Polyglyceryl-3 Methylglucose Distearate, PEG-100 Stearate, Cyclopentasiloxane, Polyhydroxystearic Acid, Butyrospermum Parkii (Shea Butter), Cyclohexasiloxane, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Stearic Acid, C12-20 Alkyl Glucoside, Dimethicone, Xanthan Gum, Aluminum Hydroxide, Decyl Glucoside, Polyethylene, Pollen Extract, Disodium EDTA, Propylene Glycol, Fragrance

Pollen UV Perfect Daily Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sunscreensunscreen

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70784-006-022021-01-29C16284748780-1ba0f9c33-241c-a910-e053-dadaa90a0b85Pollen UV Perfect Daily Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70784-006-01Pollen UV Perfect Daily Sunscreen50 mL in 1 CONTAINERCREAM502
70784-006-02Pollen UV Perfect Daily Sunscreen1 in 1 PACKAGECREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70784-006POLLEN UV PERFECT DAILY SUNSCREEN (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, OCTOCRYLENE) CREAM [NSB CO., LTD.]2Legacy NDC, 2 package rows20190108_f05d784f-4c98-44fc-a2cb-b938c81947a0.zip

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
70784-00670784-006-01, 70784-006-02

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
7ee41cd3-4622-3408-e053-2991aa0a863df05d784f-4c98-44fc-a2cb-b938c81947a02019-01-07WarningsExact identifier
spl id: 7ee41cd3-4622-3408-e053-2991aa0a863d
spl set id: f05d784f-4c98-44fc-a2cb-b938c81947a0

Reported adverse events (FAERS/openFDA)#

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