Up and Up Antiseptic

Manufacturer
Target Corporation
Effective date
2026-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:51

Label at a glance#

ProductUp and Up Antiseptic
Active ingredientCETYLPYRIDINIUM CHLORIDE
Label structure8 sections

Indications and uses

Helps prevent gingivitis, an early form of gum disease and bleeding gums Helps control plaque that leads to gingivitis and bleeding gums

Dosage and administration

Adults and Children 12 years and older: Vigorously swish 20 milliters (4 teaspoonfuls) of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse. Children 6 years to under 12 years: Supervise use. Children under 6 years: Do not use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Cetylpyridinium Chloride

Purpose

OTC - PURPOSE SECTION

Antigingivitis/Antiplaque

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent gingivitis, an early form of gum disease and bleeding gums
  • Helps control plaque that leads to gingivitis and bleeding gums

Warnings

WARNINGS SECTION

Warnings

Stop use and ask a dentist if

OTC - STOP USE SECTION

  • Gingivitis, bleeding, or redness persists for more than 2 weeks.
  • You have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease.

Keep out of reach of children under 6 years of age.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for rinsing is accidently swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children 12 years and older: Vigorously swish 20 milliters (4 teaspoonfuls) of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse.

Children 6 years to under 12 years: Supervise use.

Children under 6 years: Do not use.

Other information

OTHER SAFETY INFORMATION

  • This rinse is not intended to replace brushing or flossing
  • Do not use if the printed safety seal on the bottle's neck is missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

Citric Acid, Disodium Phosphate, Flavor, Glycerin, Lemon Oil, Poloxamer 407, Spearmint Oil, Stevia Rebaudiana, Water, Xylitol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9280792807

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1251772cetylpyridinium chloride 0.1 % Mucous Membrane Topical SolutionPSN3
1251772cetylpyridinium chloride 1 MG/ML Mucous Membrane Topical SolutionSCD3
1251772cetylpyridinium chloride 0.1 % Mucous Membrane Topical SolutionSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130191907928075GTIN-13: 0191907928075
EAN-13: 0191907928075
GTIN-12: 191907928075
UPC-A: 191907928075
GTIN storage (14 digits): 00191907928075
92807.1 Target Antiseptic.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-807-16Up and Up Antiseptic473 mL in 1 BOTTLERINSE4733

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-80782442-807-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Up and Up AntisepticCETYLPYRIDINIUM CHLORIDETarget Corporation386ee9f9-598e-ad00-e063-6394a90aeb462026-01-19WarningsExact identifier
ndc (package): 82442-807-16
ndc (product): 82442-807
ndc11 (package): 82442080716
spl id: 48c6bdb3-6cd3-7304-e063-6394a90a20a6
spl set id: 386ee9f9-598e-ad00-e063-6394a90aeb46

Reported adverse events (FAERS/openFDA)#

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