70 Dry Touch SPF 70

Manufacturer
Walgreens | Product Quiest Mfg
Effective date
2018-07-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:20

Label at a glance#

Product70 Dry Touch SPF 70
Active ingredientAvobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                     Purpose
Avobenzone-3%
Homosalate-15%                                      Sunscreen
Octisalate-5%
Octocrylene-10%
Oxybenzone-3%

INDICATIONS & USAGE SECTION

Uses Helps prevent sunburn

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Remove cap and twist up tube.
See important warnings under "When using this
product" • 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,

egularly 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-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients Adipic Acid/Diglycol Crosspolymer, Beeswax,
BHT, C12-15 Alkyl Benzoate, Caprylyl Glycol,
Fragrance, Neopentyl Glycol Diethylhexanoate,
Neopentyl Glycol Diisostearate, Octyldodecyl
Neopentanoate, Ozokerite, Paraffin, Petrolatum,
Polyester-8, Polyethylene, Silica.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-1125-012020-01-31C16284748780-19d75b9d0-bb00-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-1125-0170 Dry Touch SPF 7043 g in 1 PACKAGESTICK431

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-112570 DRY TOUCH SPF 70 (AVOBENZONE 3% HOMOSALATE 15% OCTISALATE 5% OCTOCRYLENE 10% OXYBENZONE 3%) STICK [WALGREENS]1Legacy NDC, 1 package rows20180719_9323c8fa-1707-45b3-b655-bce034ba9e21.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-11250363-1125-01

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

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
bf4e47db-46fd-47d0-9680-a53a9ee4818f9323c8fa-1707-45b3-b655-bce034ba9e212018-07-19WarningsExact identifier
spl id: bf4e47db-46fd-47d0-9680-a53a9ee4818f
spl set id: 9323c8fa-1707-45b3-b655-bce034ba9e21

Reported adverse events (FAERS/openFDA)#

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