Surface Sun SPF 50 Tropix Lotion with fragrance 2026 (IS0460-SS-V2)

Manufacturer
Surface Products Corp | Inspec Solutions LLC | Inspec Solutions LLC.
Effective date
2026-05-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:56:04

Label at a glance#

ProductSURFACE SUN SPF 50 DRY TOUCH Fragrance Free
Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE
Label structure7 sections

Indications and uses

• helps prevent sunburn • higher SPF gives more sun protection

Label contents#

Full prescribing information#

Active ingredients             Purpose          

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.00%................Sunscreen
Homosalate 10.00%..............Sunscreen
Octocrylene 6.00%................Sunscreen                   

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn • higher SPF gives more sun protection

DOSAGE & ADMINISTRATION SECTION

Directions
• apply liberally to cool, dry skin 15 minutes before sun exposure • 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 a broad spectrum SPF of 15 or higher and other sun
protection measures including: • limit time in the sun,especially from
10 a.m. - 2. p.m. • wear a long-sleeve shirts, pants, hats, and sunglasses.
• children under 6 months: Ask a doctor.

WARNINGS SECTION

Warnings
For external use only.
Do not useon damaged or broken skin.
When using this product• Keep out of eyes. Rinse with water to remove.
Stop use and ask doctor ifrash 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 immediately.

INACTIVE INGREDIENT SECTION

Inactive ingredientsAloe Barbadensis Leaf Juice, Aluminum Starch
Octenylsuccinate, Aminomethyl Propanol, Benzyl Alcohol, Butyloctyl
Salicylate, Carbomer, Dimethicone, Ethylhexylglycerin, Inulin, Lauric Acid,
Magnesium Chloride, Myristic Acid, Palmitic Acid, Phenoxyethanol,
Polyglyceryl-3 Distearate, Sodium Phytate, Sorbitan Isostearate, Sorbitol,
Stearic Acid, VP/Eicosene Copolymer, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72344-117-03SURFACE SUN SPF 50 DRY TOUCH Fragrance Free88 mL in 1 TUBELOTION882
72344-117-06SURFACE SUN SPF 50 DRY TOUCH Fragrance Free177 mL in 1 PACKAGELOTION1772

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
72344-11772344-117-03, 72344-117-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
SURFACE SUN SPF 50 DRY TOUCH Fragrance FreeHOMOSALATE 10.00% OCTOCRYLENE 6.00% AVOBENZONE 3.00%Surface Products Corp683cb489-e4e1-44ab-9543-614d42b08edd2026-05-05WarningsExact identifier
ndc (package): 72344-117-03
ndc (package): 72344-117-06
ndc (product): 72344-117
ndc11 (package): 72344011706
ndc11 (package): 72344011703
spl id: 5114fd02-1137-5f4d-e063-6394a90aeb46
spl set id: 683cb489-e4e1-44ab-9543-614d42b08edd

Reported adverse events (FAERS/openFDA)#

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