Sunscreen SPF 50

Manufacturer
Guangzhou Ariel Biotech Co., Ltd.
Effective date
2026-03-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:51:22

Label at a glance#

ProductSunscreen SPF 50
Active ingredientZINC OXIDE, SODIUM HYALURONATE, NIACINAMIDE, TITANIUM DIOXIDE
Label structure12 sections

Dosage and administration

Apply generously 15 minutes before sun exposure. Reapplication Guidelines: Reapply after 80 minutes of swimming or sweating Reapply immediately after towel drying Reapply at least every 2 hours For children under 6 months: Consult a doctor.

Storage and handling

• store at room temperature

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

15% Zinc Oxide
3% Titanium Dioxide
0.5% Niacinamide
0.5% Sodium Hyaluronate

Purpose

OTC - PURPOSE SECTION

Sunscreen
Moisturizing

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product, keep out of eyes. If contact occurs, rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if a rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Other information

STORAGE AND HANDLING SECTION

• store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Dimethicone, Glycerin, Butylene Glycol, Cyclopentasilox-
ane, Cyclohexasiloxane, Neopentyl Glycol Diheptanoate, Peg-10
Dimethicone, Lauryl Polyglyceryl-3 Polydimethylsiloxyethyl
Dimethicone,Cetyl Peg/ppg-10/1Dimethicone, Silica,
Dimethicone/phenyl Vinyl Dimethicone Crosspolymer,
Trilaureth-4 Phosphate, Magnesium Sulfate, 1,2-hexanediol,
Hydroxyacetophenone, Polyglyceryl-3 Diisostearate, Dextrin
Palmitate, Bisabolol, Niacinamide,Betaine,Triethoxycaprylylsi-
lane, Aluminum Hydroxide, Stearic Acid, Tocopheryl Acetate,
Allantoin, Anthemis Nobilis Flower Oil, Dipotassium Glycyrrhizate,
Saururus Chinensis Leaf/root Extract, Taraxacum Officinale
(Dandelion) Leaf Extract, Stephania Tetrandra Extract

Use

INDICATIONS & USAGE SECTION

Use helps prevent sunburn

Directions

DOSAGE & ADMINISTRATION SECTION

Apply generously 15 minutes before sun exposure.
Reapplication Guidelines:
Reapply after 80 minutes of swimming or sweating
Reapply immediately after towel drying
Reapply at least every 2 hours
For children under 6 months: Consult a doctor.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

undefinedundefined

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84148-021-01Sunscreen SPF 5050 g in 1 BOTTLECREAM501

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84148-02184148-021-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 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
Sunscreen SPF 50SUNSCREEN SPF 50Guangzhou Ariel Biotech Co., Ltd.4dd1b722-4448-9675-e063-6294a90a5f4f2026-03-24WarningsExact identifier
ndc (package): 84148-021-01
ndc (product): 84148-021
ndc11 (package): 84148002101
spl id: 4dd1b4d9-8bf0-9713-e063-6294a90afe8e
spl set id: 4dd1b722-4448-9675-e063-6294a90a5f4f

Reported adverse events (FAERS/openFDA)#

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