FDA.reportPublic FDA data

SPF 50 Dry Touch Continuous Spray 6 oz. - No fragrance 2026 (IS0335-SUR)

Manufacturer
Surface Products Corp | Inspec Solutions LLC | Inspec Solutions LLC.
Effective date
2026-05-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:55:53

Label at a glance#

ProductSPF 50 Dry Touch Continuous No fragrance
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE
Label structure7 sections

Indications and uses

• Helps prevent sunburn.Higher SPF gives more sun protection.

Dosage and administration

• Shake well before using spray. Spray liberally 15 minutes before sun exposure. • Reapply after 80 minutes of swimming or sweating , after towel drying, at least every 2 hours • Sun Protection Measures. Spending tme 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 includi...

Label contents#

Full prescribing information#

Active ingredients                 

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10.00%
Octisalate 5.00%
Avobenzone 3.00% 

Uses

INDICATIONS & USAGE SECTION

• Helps prevent sunburn.Higher SPF gives more sun protection.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• Shake well before using spray. Spray liberally 15 minutes before sun exposure.

• Reapply after 80 minutes of swimming or sweating , after towel drying, at least every 2 hours

• Sun Protection Measures.Spending tme 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 shirt, pants, hats, and sunglasses.
• children under 6 months: Ask a doctor.

Warnings

WARNINGS SECTION

For external use only.

Flammable:Dp not use near heat, flame or while smoking

Do not useon damage or broken skin

When using this productkeep out of eyes. Rinse with water to remove.

Do notpunncture or incinerate. Content under pressure.

Do notstore above 120F

Stop use and ask doctor ifrash occurs

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

Inactive Ingredeints

INACTIVE INGREDIENT SECTION

Alcohol Denat.
Aloe Barbadensis Leaf Juice
Butyloctyl Salicylate
Inulin
Magnesium Chloride
Oryza Sativa (Rice) Bran Oil
Polyester-8
VA/Butyl Maleate/Isobornyl Acrylate Copolymer

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
72344-111-03SPF 50 Dry Touch Continuous No fragrance170 g in 1 CANLIQUID1702

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72344-11172344-111-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ALOEV5VD430YW9IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
INULINJOS53KRJ01IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
ORYZA SATIVA (RICE) BRANR60QEP13ICIACT
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
SPF 50 Dry Touch Continuous No fragranceHOMOSALATE 10.00% OCTISALATE 5.00% AVOBENZONE 3.00%Surface Products Corp503d6b48-3516-4264-9fe8-71a9939669fe2026-05-04WarningsExact identifier
ndc (package): 72344-111-03
ndc (product): 72344-111
ndc11 (package): 72344011103
spl id: 5103af8f-4314-8fae-e063-6294a90a1c87
spl set id: 503d6b48-3516-4264-9fe8-71a9939669fe

Reported adverse events (FAERS/openFDA)#

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