AQUABAIN ANTIBACTERIAL GRAPEFRUIT- benzalkonium chloride 0.13% liquid

Aquabain Antibacterial Grapefruit by

Drug Labeling and Warnings

Aquabain Antibacterial Grapefruit by is a Otc medication manufactured, distributed, or labeled by Industria La Popular, S.A.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

to help reduce bacteria that potentially can cause disease.

Warnings

For External Use only.

When using this product

keep out of eyes, ears, and mouth, in case of contact with eyes, rinse eyes thoroughly with water

Stop use

if irritation or rash occurs. These may be signs of a serious condition.

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.

Other Information

Store between 15-30C (59-86F)

Inactive Ingredients

Aqua, Sodium Lauryl Ether Sulfate, Sodium Chloride, Cocamide MEA, Glycerin, Fragrance, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow 6, FD&C Red 40.

Aquabain Antibacterial Hand Soap Grapefruit

INGREDIENTS AND APPEARANCE

AQUABAIN ANTIBACTERIAL GRAPEFRUIT 
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62476-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.65 g  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
COCAMIDE (UNII: 3YXD33R71G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62476-003-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/01/2020

Labeler - Industria La Popular, S.A. (846044576)