Target Up and Up SPF55 Sunscreen

Manufacturer
TARGET CORPORATION
Effective date
2021-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:29

Label at a glance#

ProductTarget Up and Up SPF55 Sunscreen
Active ingredientOCTISALATE, HOMOSALATE, OCTOCRYLENE, AVOBENZONE
Label structure12 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 • children under 6 months of age: Ask a doctor • 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...

Storage and handling

• protect this product from excessive heat and direct sun • may stain or damage some fabrics, materials, or surfaces

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 15.0%

Octisalate 5.0%

Octocrylene 10.0%

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

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 if

OTC - STOP USE SECTION

• 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 Poison Control Center right away.

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

• children under 6 months of age: Ask a doctor

• 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-sleeve shirts, pants, hats, and sunglasses

Other information

STORAGE AND HANDLING SECTION

• protect this product from excessive heat and direct sun

• may stain or damage some fabrics, materials, or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

beeswax (apis mellifera), lauryl laurate, ozokerite, cetearyl behenate, polybutene, cetearyl alcohol, styrene acrylates copolymer, myristyl myristate, tocopherol (natural vitamin E), theobroma cacao (cocoa) seed butter, phenoxyethanol, retinyl palmitate (vitamin A), tetrahexyldecyl ascorbate (vitamin C)

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8222282222

82404E282404E2

82404V182404V1

82408E82408E

82408K82408K

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-12811673-128-56, 11673-128-57

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
247611a4-16ff-ad04-e063-6394a90a6455bd0ed7f2-7e94-d99a-e053-2995a90a5cad2024-10-14WarningsExact identifier
spl set id: bd0ed7f2-7e94-d99a-e053-2995a90a5cad

Reported adverse events (FAERS/openFDA)#

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