TARGET UP AND UP FOAMING BODY WASH ACNE TREATMENT

Manufacturer
TARGET CORPORATION
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:52:35

Label at a glance#

ProductTARGET UP AND UP FOAMING BODY WASH ACNE TREATMENT
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the treatment of acne.

Dosage and administration

cover the entire affected area with a thin layer and rinse thoroughly 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 a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2.0%

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • cover the entire affected area with a thin layer and rinse thoroughly 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 a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other information

OTHER SAFETY INFORMATION

  • may stain some fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, sodium C14-16 olefin sulfonate, glycerin, cocamidopropyl betaine, acrylates copolymer, cocamidopropyl PG-dimonium chloride phosphate, polyquaternium-7, citrus grandis (grapefruit) fruit extract, anthemis nobilis flower extract (roman chamomile), camellia sinensis leaf extract (green tea), chondrus crispus powder (carrageenan), agar, neopentyl glycol dicaprylate/dicaparate, sodium ascorbyl phosphate (vitamin C phosphate), propylene glycol, C12-15 alkyl lactate, polysorbate 20, butylene glycol, polyvinyl alcohol, potassium chloride, phenethyl alcohol, PPG-2 methyl ether, disodium EDTA, sodium chloride, sodium hydroxide, benzlkonium chloride, sodium benzotriazolyl butylphenol sulfonate, fragrance, mica, titanium dioxid, iron oxides, red 30, red 40, ext. violet 2

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TARGET UP & UP FOAMING BODY WASH ACNE TREATMENT

8.5 FL OZ (251mL)

NDC 11673-981-55

82537E2F482537E2F4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-981TARGET UP AND UP FOAMING BODY WASH ACNE TREATMENT (SALICYLIC ACID) LIQUID [TARGET CORPORATION]3Legacy NDC20241016_badb390f-6486-c07c-e053-2995a90a3024.zip

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-98111673-981-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 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
2476d673-7d87-029a-e063-6294a90a1c02badb390f-6486-c07c-e053-2995a90a30242024-10-14WarningsExact identifier
spl id: 2476d673-7d87-029a-e063-6294a90a1c02
spl set id: badb390f-6486-c07c-e053-2995a90a3024

Reported adverse events (FAERS/openFDA)#

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