FDA.reportPublic FDA data

Up & Up 311.007/311AK-AN

Manufacturer
Target Corporation | Nice-Pak Products, LLC
Effective date
2026-04-21
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-06-01 01:54:29

Label at a glance#

Product2 in 1 Dandruff
Active ingredientPYRITHIONE ZINC
Label structure13 sections

Dosage and administration

shake well for maximum dandruff control, use every time you shampoo wet hair, massage onto scalp, rinse, repeat if desired for best results use at least twice a week or as directed by a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

helps prevent recurrence of flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use as directed

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

  • shake well
  • for maximum dandruff control, use every time you shampoo
  • wet hair, massage onto scalp, rinse, repeat if desired
  • for best results use at least twice a week or as directed by a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, sodium xylenesulfonate, amodimethicone, cocamidopropyl betaine, fragrance, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, citric acid, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

Questions?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Procter & Gamble, distributor of Head & Shoulders Classic Clean 2-in-1 Dandruff Shampoo + Conditioner.

Adverse Reactions

ADVERSE REACTIONS SECTION

Dist. by Target Corp., Mpls., MN 55403

Made in the U.S.A. with U.S. and foreign components

TM & © 2025 Target Brands, Inc.

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11673-643-11

Compare to Head & Shoulders ®2-in-1 Classic Clean Dandruff Shampoo + Conditioner*

Antidandruff Shampoo & Conditioner with 1% Pyrithione Zinc

Helps relieve dryness, itching and flaking associated with dandruff

Two-in-One

up&up™

22 FL OZ (1.37 PT) 651 mL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN16
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD16
209884zinc pyrithione 1 % Medicated ConditionerSY16
209884zinc pyrithione 1 % Medicated ShampooSY16

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0021571BCmm02.jpg
Data codeData MatrixL0021571FCmm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-643-112 in 1 Dandruff651 mL in 1 BOTTLE, PLASTICSHAMPOO65116
11673-643-862 in 1 Dandruff1000 mL in 1 BOTTLE, PLASTICSHAMPOO100016

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-64311673-643-86, 11673-643-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
MAGNESIUM CARBONATE HYDROXIDEYQO029V1L4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB
WATER059QF0KO0RIACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM CHLORIDE451W47IQ8XIACT
ZINC CARBONATEEQR32Y7H0MIACT
SODIUM XYLENESULFONATEG4LZF950URIACT
AMODIMETHICONE (800 CST)363Z2T48P7IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM BENZOATEOJ245FE5EUIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
152026-02-18monthly-update2026-06-03 17:56:36

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
2 in 1 DandruffPYRITHIONE ZINCTarget Corporationa9d92e08-a77f-45dd-b95a-9923202df40b2026-04-21Warnings, Adverse reactionsExact identifier
ndc (package): 11673-643-86
ndc (package): 11673-643-11
ndc (product): 11673-643
ndc11 (package): 11673064386
ndc11 (package): 11673064311
spl id: 4ffd8965-0869-09db-e063-6394a90a9ba2
spl set id: a9d92e08-a77f-45dd-b95a-9923202df40b

Reported adverse events (FAERS/openFDA)#

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