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Ultra by DOLGENCORP, LLC

Dosage form: liquid
Ingredients: CHLOROXYLENOL 3.09g in 1mL
Labeler: DOLGENCORP, LLC
NDC Code: 55910-589

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

drug facts

claims

WARNING

NOT FOR USE IN DISHWASHERS.

DO NOT ADD BLEACH

Phosphate Free   Contains Surfactamts

When compared to non-concentrated formulas

This product is not manufactured or distributed by Procter & Gamble,

distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom

Active ingredient

Chloroxylenol 0.3%

Purpose

Antibacterial

Use

 for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product
  • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if
  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions
  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, sodium C14-16 olefin sulfonate, lauramine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium xylenesulfonate, sodium chloride, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, yellow 5, blue 1

ADVERSE REACTIONS

DISTRIBUTED BY DOLGENCORP, LLC

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

PACKAGE LABEL

ULTRA CONCENTRATED 2X CLEANING POWER

DG home

Ultra

Antibacterial

Hand Soap

Dishwashing Liquid

TOUGH ON GREASE

Compare to Dawn Ultra

Antibacterial Hand Soap

Apple Blossom Scent

18 FL OZ (532 mL)

ULTRA 
chloroxylenol 0.3% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-589
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL3.09 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
SODIUM C14-16 OLEFIN SULFONATE 
LAURAMINE OXIDE 
SODIUM LAURETH SULFATE 
SODIUM LAURYL SULFATE 
SODIUM XYLENESULFONATE 
SODIUM CHLORIDE 
ALCOHOL 
PHENOXYETHANOL 
CITRIC ACID MONOHYDRATE 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:55910-589-44709 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/17/2017
Labeler - DOLGENCORP, LLC (068331990)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(55910-589)

Revised: 01/2017
 
DOLGENCORP, LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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