DISHWASHING LIQUID AND ANTIBACTERIAL HAND ORANGE SCENT ULTRA CONCENTRATED- chloroxylenol solution

Dishwashing Liquid and Antibacterial Hand by

Drug Labeling and Warnings

Dishwashing Liquid and Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Mid-Continent Packaging Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Inactive ingredients

Water, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Sodium Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yellow No. 5, D&C Red No. 33.

Questions?

1-888-723-3929

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY
BETTER LIVING BRANDS LLC
P.O. BOX 99
PLEASANTON, CA 94566-0009

PRINCIPAL DISPLAY PANEL - 709 mL Bottle Label

Signature™
HOME
QUALITY GUARANTEED

Dishwashing Liquid &
Antibacterial Hand Soap

orange scent
ULTRA
Concentrated

CAUTION: KEEP OUT OF REACH
OF CHILDREN. See warning on back label.

24 FL OZ (1.5 PT) 709 mL

490009787

INGREDIENTS AND APPEARANCE

DISHWASHING LIQUID AND ANTIBACTERIAL HAND   ORANGE SCENT ULTRA CONCENTRATED
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69560-123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
EDETATE SODIUM (UNII: MP1J8420LU)
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69560-123-01	709 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/10/2020

Labeler - Mid-Continent Packaging Inc. (798250239)