Target Up & Up Daily Moisturizing Lotion

Manufacturer
TARGET CORPORATION
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:25:26

Label at a glance#

ProductTarget Up and Up Daily Moisturizing
Active ingredientDIMETHICONE
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 as needed to hands or body when skin feels dry or irritated

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 1.2%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

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 - WHEN USING SECTION

• deep or puncture wounds • animal bites • serious burns

When using this product

OTC - DO NOT USE SECTION

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

• condition worsens • symptoms last more than seven days or clear up and occur again within a few days

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 as needed to hands or body when skin feels dry or irritated

Other information

OTHER SAFETY INFORMATION

  • may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

avena sativa (oat) kernel flour, behenrimonium chloride, benzyl alcohol, cetearyl alcohol, cetyl alcohol, glycerin, isopropyl palmitate, petrolatum, polyquaterium-37, sodium chloride, water.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82845E8F982845E8F9

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
876980dimethicone 1.2 % Topical LotionPSN4
876980dimethicone 12 MG/ML Topical LotionSCD4
876980dimethicone 1.2 % Topical LotionSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-087-18Target Up and Up Daily Moisturizing85 mL in 1 TUBELOTION854
11673-087-43Target Up and Up Daily Moisturizing532 mL in 1 BOTTLELOTION5324
11673-087-98Target Up and Up Daily Moisturizing2 in 1 PACKAGELOTION24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-087TARGET UP AND UP DAILY MOISTURIZING (DIMETHICONE) LOTION [TARGET CORPORATION]4Current NDC, Legacy NDC, 3 package rows20241016_f118e0eb-1e66-50ab-e053-2995a90a2cb9.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-08711673-087-18, 11673-087-43, 11673-087-98

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
Target Up and Up Daily MoisturizingDIMETHICONETARGET CORPORATIONf118e0eb-1e66-50ab-e053-2995a90a2cb92024-10-14WarningsExact identifier
ndc (package): 11673-087-98
ndc (package): 11673-087-18
ndc (package): 11673-087-43
ndc (product): 11673-087
ndc11 (package): 11673008743
ndc11 (package): 11673008718
ndc11 (package): 11673008798
spl id: 2475ef86-7ed0-734a-e063-6394a90a6ddd
spl set id: f118e0eb-1e66-50ab-e053-2995a90a2cb9

Reported adverse events (FAERS/openFDA)#

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