UP AND UP MEDICATED ANTI-DANDRUFF  ANTI-DANDRUFF, ANTI-SEBORRHEIC DERMATITIS, ANTI-PSORIASIS- selenium sulfide shampoo 
TARGET CORPORATION

----------

up & up Medicated Anti-dandruff Shampoo
Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis

Drug Facts

Active ingredient

Selenium sulfide 1%

Purpose

Anti-Seborrheic Dermatitis, anti-dandruff

Uses

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

Warnings

For external use only.

Ask a doctor before use if

  • condition covers a large area of the body.

When using this product

  • 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

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

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

Directions

Other information

Inactive ingredients

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?

1-866-567-8600

Dist. by Target Corporation
Minneapolis, MN 55403

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label

Anti-dandruff Shampoo
with 1% Selenium Sulfide

Dermatologist
Tested

up&up

12 FL OZ (355 mL)

Medicated

05-4718

PRINCIPAL DISPLAY PANEL - 355 mL Bottle Label
UP AND UP MEDICATED ANTI-DANDRUFF   ANTI-DANDRUFF, ANTI-SEBORRHEIC DERMATITIS, ANTI-PSORIASIS
selenium sulfide shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-384
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
AMMONIUM LAURETH-5 SULFATE (UNII: 43ZIH89I48)  
Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
Glycerin (UNII: PDC6A3C0OX)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Chlorphenesin (UNII: I670DAL4SZ)  
Sodium Hydroxide (UNII: 55X04QC32I)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Sodium Chloride (UNII: 451W47IQ8X)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Product Characteristics
ColorGREENScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-384-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM03204/04/2024
Labeler - TARGET CORPORATION (006961700)
Registrant - Garcoa, Inc. (036464697)
Establishment
NameAddressID/FEIBusiness Operations
Sigan Industries INC255106239MANUFACTURE(82442-384) , LABEL(82442-384) , PACK(82442-384)

Revised: 4/2024
Document Id: bd55b3fe-6c2f-459b-845f-064bf1dad460
Set id: a516282f-ed6b-4e94-b269-ea34f700dd69
Version: 2
Effective Time: 20240425
 
TARGET CORPORATION