JABONITO KIDS GREEN APPLE LIQUID- benzalkonium chloride 0.13% liquid

Jabonito Kids Green Apple Liquid by

Drug Labeling and Warnings

Jabonito Kids Green Apple Liquid 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

Antibacterial

Uses

For washing to decrease bacteria on the skin

Warnings

For External Use only.

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

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.

Other Information

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

Inactive Ingredients

Aqua, Sodium Lauryl Ether Sulfate, Sodium Chloride, Cocamide MEA, Phenoxyethanol, Fragrance (Parfum), Methylchloroisothiazolinone/Methylisothiazolinone, Citric Acid, FD&C Yellow No. 5, FD&C Blue No. 1.

Jabonito Kids Green Apple Liquid Hand Soap

INGREDIENTS AND APPEARANCE

JABONITO KIDS GREEN APPLE LIQUID 
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62476-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.31 g  in 237 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM LAURYL ETHOXYSULFATE (UNII: SUY7YR7K8F)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62476-009-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/01/2023

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