FDA.reportPublic FDA data

ULTA SUN DRY TOUCH SPF 70

Manufacturer
Ulta
Effective date
2016-01-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:45:34

Label at a glance#

ProductULTA SUN DRY TOUCH SPF 70
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure8 sections

Indications and uses

helps prevent sunburn 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 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#

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE 3.0%, HOMOSALATE 15.0%, OCTISALATE 5.0%, OCTOCRYLENE 2.8%,

OXYBENZONE 6.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION


  • helps prevent sunburn
  • 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 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

OTC - ASK DOCTOR SECTION

if rash occurs

Keep out of the 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.

  • May stain some fabrics

Directions

DOSAGE & ADMINISTRATION 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 10:00 a.m. - 2 p.m.
  • wear long-sleeve shirts, pants, hats and sunglasses
  • children under 6 months of age: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Styrene/Acrylates Copolymer, Butyloctyl Salicylate, Silica, Glyceryl Stearate, PEG-100 Stearate, Caprylyl Methicone, Sodium Polyacrylate, Benzyl Alcohol, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Ethylhexyl Stearate, Beeswax, Dimethicone, Chlorphenesin, Cetyl Dimethicone, Xanthan Gum, Trimethylsiloxysilicate, Fragrance, Trideceth-6, Disodium EDTA, BHT, Dipotassium Glycyrrhizate.

Other information

SPL UNCLASSIFIED SECTION

  • protect this product from excessive heat and direct sun

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


62296-8900-4

SUNCARE

BROAD SPECTRUM

SPF 70

WATER RESISTANT

(80 MINUTES)

LIGHT WEIGHT

SUNSCREEN LOTION

SHEER

ULTA

5 fl oz/147 ml


Label
Label






DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62296-8900-42020-01-31C16284748780-19d75b9d0-7771-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62296-8900-4ULTA SUN DRY TOUCH SPF 70147 g in 1 BOTTLELOTION1472

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62296-8900ULTA SUN DRY TOUCH SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]2Legacy NDC, 1 package rows20160330_4a89873c-7339-428d-8b67-7b96ef5c5b1b.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62296-890062296-8900-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OXYBENZONE95OOS7VE0YACTIB
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
BENZYL ALCOHOLLKG8494WBHIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
YELLOW WAX2ZA36H0S2VIACT
DIMETHICONE92RU3N3Y1OIACT
CHLORPHENESINI670DAL4SZIACT
XANTHAN GUMTTV12P4NEEIACT
TRIDECETH-63T5PCR2H0CIACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT

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
b867b4e9-4c23-4226-bebe-8df4050639734a89873c-7339-428d-8b67-7b96ef5c5b1b2016-01-25WarningsExact identifier
spl id: b867b4e9-4c23-4226-bebe-8df405063973
spl set id: 4a89873c-7339-428d-8b67-7b96ef5c5b1b

Reported adverse events (FAERS/openFDA)#

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