FDA.reportPublic FDA data

Target Up and Up SPF 50 Sunscreen

Manufacturer
TARGET CORPORATION
Effective date
2024-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:20:07

Label at a glance#

ProductTarget Up and Up SPF 50 Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
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 value of 15 or higher and...

Storage and handling

• protect the product in this container 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 7.0%

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 - ASK DOCTOR SECTION

rash 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

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 value 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

Other information

STORAGE AND HANDLING SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aluminum starch octenylsuccinate, aminomethyl propanol, benzyl alcohol, butyrospermum parkii (shea) butter, caprylyl glycol, carbomer, dimethicone, disodium EDTA, ethylhexylglycerin, fragrance, persea gratissima (avocado) oil, phenoxyethanol, polyethyloxazoline, polyglyceryl-3 distearate, simmondsia chinensis (jojoba) seed oil, sorbitan isostearate, sorbitol, stearic acid, tocopherol, tridecyl salicylate, water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82947A82947A

82949A82949A

82954EF82954EF

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-005-12Target Up and Up SPF 50 Sunscreen237 mL in 1 TUBELOTION2371
82442-005-68Target Up and Up SPF 50 Sunscreen473 mL in 1 BOTTLELOTION4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-005TARGET UP AND UP SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [TARGET CORPORATION]1Current NDC, 2 package rows20240926_22e359cd-4c63-b124-e063-6394a90aec73.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-00582442-005-12, 82442-005-68

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBITAN ISOSTEARATE01S2G2C1E4IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
BENZYL ALCOHOLLKG8494WBHIACT
CAPRYLYL GLYCOL00YIU5438UIACT
HEXAMETHYLDISILOXANED7M4659BPUIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
SORBITOL506T60A25RIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
STEARIC ACID4ELV7Z65APIACT
WATER059QF0KO0RIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
(C10-C30)ALKYL METHACRYLATE ESTERXH2FQZ38D8IACT
TOCOPHEROLR0ZB2556P8IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
AVOCADO OIL6VNO72PFC1IACT
JOJOBA OIL724GKU717MIACT
SHEA BUTTERK49155WL9YIACT
POLYETHYLOXAZOLINE (200000 MW)I765I75FT2IACT
POLYGLYCERYL-3 DISTEARATEZI1LK470XVIACT

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
Target Up and Up SPF 50 SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENETARGET CORPORATION22e359cd-4c63-b124-e063-6394a90aec732024-09-24WarningsExact identifier
ndc (package): 82442-005-68
ndc (package): 82442-005-12
ndc (product): 82442-005
ndc11 (package): 82442000568
ndc11 (package): 82442000512
spl id: 22e3522b-03e0-8c50-e063-6394a90a9725
spl set id: 22e359cd-4c63-b124-e063-6394a90aec73

Reported adverse events (FAERS/openFDA)#

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