MERINGUE FOAMING DYE FREE ANTIBACTERIAL- choroxylenol liquid

Meringue Foaming Dye Free Antibacterial by

Drug Labeling and Warnings

Meringue Foaming Dye Free Antibacterial by is a Otc medication manufactured, distributed, or labeled by United Laboratories Inc., Woodbine Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Chloroxylenol 0.25%

Purpose

Antibacterial

Uses:

For hand washing to decrease bacteria on the skin.

Warnings:

For external use only

When using this productavoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor ifirritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.Children must be surpervised in use of this product. If swallowed, get medical help or contact a Poison Control center right away.

Directions:

For maximum efficiency, pump foam into dry hands, later vigorously for 30 seconds, rinse and dry.

Other Information:

Store at 20 to 25 C [68 to 77 F]

Inactive ingredients:

Water, Sodium Lauryl Ether Sulfate, Decyl Glucoside, Cocamidopropyl Betaine, Fragrance, Propylene Glycol and Preservative

PRINCIPAL DISPLAY PANEL

UNITED

Laboratories

United 758

MERINGUE

Foaming Dye Free

Antibacterial

Hand Soap

750 ml (25 fl.oz.) Made in USA 1018

INGREDIENTS AND APPEARANCE

MERINGUE FOAMING DYE FREE ANTIBACTERIAL 
choroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63998-758
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63998-758-01	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/22/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/22/2022

Labeler - United Laboratories Inc. (001759737)

Establishment
Name	Address	ID/FEI	Business Operations
Woodbine Products Company		004220323	manufacture(63998-758)