Up and Up

Manufacturer
TARGET CORPORATION
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:25:18

Label at a glance#

ProductUp and Up Deep Clean Toner
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the treatment of acne.

Dosage and administration

• clean the skin thoroughly before using this product • cover the entire affected area with a thin layer one to three times daily • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Storage and handling

• may stain some fabric

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.5%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

  • for the treatment of acne.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

• skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs only use one topical acne medication at a time. • avoid contact with eyes. If contact occurs, flush thoroughly with water.

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

• clean the skin thoroughly before using this product • cover the entire affected area with a thin layer one to three times daily • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

STORAGE AND HANDLING SECTION

• may stain some fabric

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol denat. (24.5 %), glycerin, isoceteth-20, PEG-32, sodium citrate, fragrance, propylene glycol, dimethicone propyl PG-betaine, benozphenone-4, algae extract, aloe barbadenis leaf juice, blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Up & Up Deep Clean Toner

8 FL OZ (236.5 mL)

NDC 11676-936-11

82378E382378E3

82378F482378F4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199308salicylic acid 0.5 % Topical SolutionPSN5
199308salicylic acid 5 MG/ML Topical SolutionSCD5
199308salicylic acid 0.5 % Topical SolutionSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-936-11Up and UpDeep Clean Toner236.5 mL in 1 BOTTLELIQUID236.55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-936UP AND UP DEEP CLEAN TONER (SALICYLIC ACID) LIQUID [TARGET CORPORATION]5Current NDC, Legacy NDC, 1 package rows20241016_945b0588-6864-27bc-e053-2995a90a73e3.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-93611673-936-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
Up and Up Deep Clean TonerSALICYLIC ACIDTARGET CORPORATION945b0588-6864-27bc-e053-2995a90a73e32024-10-14WarningsExact identifier
ndc (package): 11673-936-11
ndc (product): 11673-936
ndc11 (package): 11673093611
spl id: 24765a58-28ea-4a93-e063-6394a90a352f
spl set id: 945b0588-6864-27bc-e053-2995a90a73e3

Reported adverse events (FAERS/openFDA)#

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