FDA.reportPublic FDA data

up and up Medicated Anti-dandruff

Manufacturer
TARGET CORPORATION | Garcoa, Inc. | SV Labs Toronto Corporation
Effective date
2024-04-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:17:54

Label at a glance#

Productup and up Medicated Anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis
Active ingredientSELENIUM SULFIDE
Label structure11 sections

Indications and uses

for the relief of flaking, and itching associated with dandruff, and seborrheic dermatitis and to help prevent recurrence.

Dosage and administration

shake well shampoo, then rinse thoroughly for best results, use at least twice a week or as directed by a doctor.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Selenium sulfide 1%

Purpose

OTC - PURPOSE SECTION

Anti-Seborrheic Dermatitis, anti-dandruff

Uses

INDICATIONS & USAGE SECTION

for the relief of flaking, and itching associated with dandruff, and seborrheic dermatitis and to help prevent recurrence.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

  • condition covers a large area of the body.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
  • for color-treated or permed hair, rinse thoroughly.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • shampoo, then rinse thoroughly
  • for best results, use at least twice a week or as directed by a doctor.

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, ammonium lauryl sulfate, ammonium laureth sulfate, cocamide MIPA, cocamidopropyl betaine, acrylates copolymer, glycerin, menthol, magnesium aluminum silicate, fragrance, phenoxyethanol, chlorphenesin, sodium hydroxide, citric acid, sodium chloride, blue 1, red 33.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-567-8600

SPL UNCLASSIFIED SECTION

Dist. by Target Corporation
Minneapolis, MN 55403

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Anti-dandruff Shampoo
with 1% Selenium Sulfide

  • Helps eliminate
    recurrence of scalp
    itching and flaking
  • Infused with
    cooling menthol

Dermatologist
Tested

up&up™

12 FL OZ (355 mL)

Medicated

05-4718

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204642selenium sulfide 1 % Medicated ShampooPSN3
204642selenium sulfide 10 MG/ML Medicated ShampooSCD3
204642selenium sulfide 1 % Lotion ShampooSY3
204642selenium sulfide 1 % Medicated ShampooSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-384-01up and up Medicated Anti-dandruffAnti-dandruff, anti-seborrheic dermatitis, anti-psoriasis355 mL in 1 BOTTLESHAMPOO3553

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-38482442-384-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
SELENIUM SULFIDEZ69D9E381QACTIB
Water059QF0KO0RIACT
AMMONIUM LAURETH-5 SULFATE43ZIH89I48IACT
Ammonium Lauryl SulfateQ7AO2R1M0BIACT
COCO MONOISOPROPANOLAMIDE21X4Y0VTB1IACT
Cocamidopropyl Betaine5OCF3O11KXIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
GlycerinPDC6A3C0OXIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
Magnesium Aluminum Silicate6M3P64V0NCIACT
PhenoxyethanolHIE492ZZ3TIACT
ChlorphenesinI670DAL4SZIACT
Sodium Hydroxide55X04QC32IIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
Sodium Chloride451W47IQ8XIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT

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 Medicated Anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasisSELENIUM SULFIDETARGET CORPORATIONa516282f-ed6b-4e94-b269-ea34f700dd692024-04-25WarningsExact identifier
ndc (package): 82442-384-01
ndc (product): 82442-384
ndc11 (package): 82442038401
spl id: f1856542-23c1-48ca-921a-62d9b42ac5a8
spl set id: a516282f-ed6b-4e94-b269-ea34f700dd69

Reported adverse events (FAERS/openFDA)#

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