ANTIBACTERIAL HAND- benzalkonium chloride soap

ANTIBACTERIAL HAND by

Drug Labeling and Warnings

ANTIBACTERIAL HAND by is a Otc medication manufactured, distributed, or labeled by Pride Products Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE (0.13% M/M)

PURPOSE

ANTIMICROBIAL

USES

SIMPLY SOFT LIQUID SOAP CLEANS HANDS WITHOUT DRYING YOUR SKIN. PERFECT FOR ALL SKIN TYPES.

WARNINGS

KEEP AWAY FROM DIRECT SUNLIGHT. IN CASE OF CONTACT WITH EYES, RINSE EYES WITH PLENTY OF WATER.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DIRECTIONS

WET YOUR HANDS WITH CLEAN WATER. FILL OPEN PALM WITH ONE PUMPFUL OF SIMPLY SOFT LIQUID SOAP. LATHER YOUR HANDS BY RUBBING THEM TOGETHER WITH THE SOAP. RINSE YOUR HANDS UNDER CLEAN, RUNNING WATER.

INACTIVE INGREDIENTS

AQUA (WATER), LAURYL GLUCOSIDE, COCAMIDOPROPYL BETAINE, LAURAMINE OXIDE, GLYCERIN, PEG 120 METHYL GLUCOSE DIOLEATE, CITRIC ACID, PARFUM, TETRASODIUM EDTA, BENZYL ALCOHOL, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, LIMONENE, CITRAL, FD&C YELLOW NO. 6, D&C RED NO. 33.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58037-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
EDETATE SODIUM (UNII: MP1J8420LU)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CITRAL (UNII: T7EU0O9VPP)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58037-104-11	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/06/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/06/2021

Labeler - Pride Products Corp. (109020099)