Sunplus SPF 30 Mist Sunscreen

Manufacturer
SUNPLUS SKIN CARE LLC | Pure Source, LLC
Effective date
2026-10-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-10-22 02:02:25

Label at a glance#

ProductSunplus SPF 30 Mist Sunscreen
Active ingredientAVOBENZONE, OCTISALATE, OCTOCRYLENE
Label structure8 sections

Indications and uses

• Helps prevent sunburn. • higher SPF gives more sunburn protection • retains SPF after 80 minutes of swimming or sweating • 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 and as needed. • Children under 6 months of age: ask a doctor. • Reapply: • after 80 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 this risk, regularly use a sunscreen with broad-spectrum SPF of 15 or h...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.00%
Octisalate 5.00%
Octocrylene 10.00%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses:

INDICATIONS & USAGE SECTION

• Helps prevent sunburn. • higher SPF gives more sunburn protection • retains SPF after 80 minutes of swimming or sweating • 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 use

OTC - DO NOT USE SECTION

  • on damaged or 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

  • a rash or irritation develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use

Directions:

DOSAGE & ADMINISTRATION SECTION

• Apply liberally 15 minutes before sun exposure and as needed. • Children under 6 months of age: ask a doctor. • Reapply: • after 80 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 this risk, regularly use a sunscreen with broad-spectrum SPF of 15 or higher and other sun protection measures, including: • Limit time in the sun, especially from 10 a.m. to 2 p.m. •Wear long-sleeved shirts, pants, hats, and sunglasses.

Other Information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Alcohol, Butyloctyl Salicylate, Methyl Dihydroabietate, Actinidia Chinensis (Kiwi) Fruit Extract, Lycium Barbarum Fruit Extract, Punica Granatum Extract, Garcinia Mangostana (Mangosteen) Extract, Aloe Barbadensis Leaf Extract, Helianthus Annuus (Sunflower) Seed Oil, Tocopheryl Acetate, Glycerin, Water (Aqua), Ascorbyl Palmitate, Carthamus Tinctorius (Safflower) Seed Oil, Cocos Nucifera (Coconut) Oil, Linum Usitatissimum (Linseed) Seed Oil, Fragrance (Parfum)

QUESTIONS?

OTC - QUESTIONS SECTION

info@sunplus.com or sunplusca.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860014830747GTIN-13: 0860014830747
EAN-13: 0860014830747
GTIN-12: 860014830747
UPC-A: 860014830747
GTIN storage (14 digits): 00860014830747
Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84661-02084661-020-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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