ULTRA- chloroxylenol 0.3% liquid

Ultra by

Drug Labeling and Warnings

Ultra by is a Otc medication manufactured, distributed, or labeled by Aldi, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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, tetrasodium EDTA, yellow 5, blue 1

SPL UNCLASSIFIED SECTION

WARNING

NOT FOR USE IN DISHWASHERS.

DO NOT ADD BLEACH

Phosphate Free Contains Surfactants

Not tested on animals

ANTIBACTERIAL

HAND SOAP

GREEN APPLE SCENT

Ultra Concentrated

Dishwashing Liquid

DIST. & SOLD EXCLUSIVELY BY:

ALDI, BATAVIA, IL 60510

This product is not manufactured or distributd by Procter & Gamble,  distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent

principal display panel

Radiance

TOUCH ON GREASE

ANTIBACTERIAL | HAND SOAP

COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP APPLE BLOSSOM SCENT

24 FL OZ (710 mL)

INGREDIENTS AND APPEARANCE

ULTRA 
chloroxylenol 0.3% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64024-956
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3.09 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64024-956-44	710 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/17/2019

Labeler - Aldi (944259522)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(64024-956)