Surface Sun Dry Touch SPF 30 Sunscreen

Manufacturer
Surface Products Corp | CGI Packaging, LLC
Effective date
2018-05-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:55:43

Label at a glance#

ProductSurface Sun Dry Touch SPF 30 Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure8 sections

Dosage and administration

Apply liberally 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...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 2%, Oxybenzone 2.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

DOSAGE & ADMINISTRATION SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse eyes with water to remove. Stop use and ask a doctor if rash occurs.

Keep Out of Reach of Children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

Apply liberally 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 long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months: ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

1,2-Hexanediol, Behenyl Alcohol, BHT, Butyloctyl Salicylate, Calcium Pantothenate, Caprylyl Glycol, Caprylyl Methicone, Dimethicone, Dimethyl Capramide, Disodium EDTA, Ethylhexyl Stearate, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hydrated Silica, Lecithin, Lepidium Sativum Sprout Extract, Maltodextrin, Niacinamide, PEG-100 Stearate, Polyester-8, Pyridoxine HCl, Silica, Sodium Ascorbyl Phosphate, Sodium Polyacrylate, Sodium Starch Octenylsuccinate, Styrene/Acrylates Copolymer, Tocopheryl Acetate, Trideceth-6, Trimethylsiloxysilicate, VP/Hexadecene Copolymer, Water, Xanthan Gum.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Surface Sun Dry Touch SPF 30Surface Sun Dry Touch SPF 30Surface Sun Dry Touch SPF 30Surface Sun Dry Touch SPF 30

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72344-009-032020-01-31C16284748780-19d75b9cf-fa67-f424-e053-dadaa90a57ce6d70e7c4-eddf-c161-e053-2991aa0ad324
72344-009-062020-01-31C16284748780-19d75b9cf-fa67-f424-e053-dadaa90a57ce6d70e7c4-eddf-c161-e053-2991aa0ad324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72344-009-03Surface Sun Dry Touch SPF 30 Sunscreen88.7 mL in 1 TUBELOTION88.72
72344-009-06Surface Sun Dry Touch SPF 30 Sunscreen177 mL in 1 TUBELOTION1772

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72344-009SURFACE SUN DRY TOUCH SPF 30 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [SURFACE PRODUCTS CORP]2Legacy NDC, 2 package rows20180531_6d70e7c4-eddf-c161-e053-2991aa0ad324.zip

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72344-00972344-009-06, 72344-009-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 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
6d72685d-ec8e-5d62-e053-2a91aa0a54f06d70e7c4-eddf-c161-e053-2991aa0ad3242018-05-30WarningsExact identifier
spl id: 6d72685d-ec8e-5d62-e053-2a91aa0a54f0
spl set id: 6d70e7c4-eddf-c161-e053-2991aa0ad324

Reported adverse events (FAERS/openFDA)#

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