TARGET UP AND UP ACNE SPOT TREATMENT

Manufacturer
TARGET CORPORATION
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:19:26

Label at a glance#

ProductTARGET UP AND UP ACNE SPOT TREATMENT
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

For the treatment of acne

Dosage and administration

Cleanse skin thoroughly before applying product. Cover the entire afffected 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 a doctor If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2.0%

Purpose

OTC - PURPOSE SECTION

Acne Medication

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.

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. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Cleanse skin thoroughly before applying product.
  • Cover the entire afffected 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 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

alcohol denat., ammonium hydroxide, benzalkonium chloride, butylene glycol, C12-15 alkyl lactate, C13-14 isoparaffin, capryloyl glycine, cedrus atlantica bark extract, cetyl lactate, cinnamomum zeylanicum bark extract, cocamidopropyl PG-dimonium chloride phosphate, cyclopentasiloxane, dehydroxanthan gum, ethylparaben, fragrance, glycerin, hamamelis virginiana (witch hazel) extract, hexylene glycol, laureth-7, methylparaben, phenethyl dimethicone, phenoxyethanol, polyacrylamide, polysorbate 20, portulaca oleracea extract, PPG-2 isocetheth-20 acetate, propylparaben, sarcosine, tetrasodium EDTA, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

823995K5823995K5

82399A482399A4

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-13811673-138-51, 11673-138-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
24763776-e3be-0ca6-e063-6294a90a1da1d4c70db3-69c5-727d-e053-2995a90a769e2024-10-14WarningsExact identifier
spl set id: d4c70db3-69c5-727d-e053-2995a90a769e

Reported adverse events (FAERS/openFDA)#

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