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

Methylcloroisothiazolinone/Methylisothiazolinone, Sodium Benzotriazolyl Butylphenol Sulfonate/Buteth-3/Tributyl Citrate, FD&C Red No. 40, FD&C Yellow No. 5.

DK12 Liquid Hand Soap Creamy

label label

DK12 LIQUID HAND CREAMY
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62476-008
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
BUTETH-3 (UNII: OC116GRO69)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
TRIBUTYL CITRATE (UNII: 827D5B1B6S)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62476-008-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2023

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

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