DK12 SHOWER GEL CREAMY- benzalkonium chloride 0.13% gel

DK12 Shower Gel Creamy by

Drug Labeling and Warnings

DK12 Shower Gel Creamy 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

Apply to a body sponge on damp skin, rub into a rich lather all over the body, then rinse thoroughly.

Other Information

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

Inactive Ingredients

Aqua, Sodium Lauryl Ether Sulfate, Cocamidopropyl B e t a i n e , L a u r y l G l u c o s i d e , G l y c o l
Distearate/Laureth-4/Cocamidopropyl Betaine, Decyl Glucoside (and) Cocamidopropyl Hydroxysultaine (and) Cocamidopropyl Betaine (and) Cocamide MIPA (and) Disodium Laureth Sulfosuccinate (and) Disodium Lauryl Sulfosuccinate, Cocamidopropyl Betaine (and) Lauramide MIPA, Propylene Glycol, Disodium Cocoamphodiacetate, Sodium Lauryl Sarcosinate, Sodium Chloride, Jojoba Wax PEG-120 Esters, Aqua/Pentylene G l y c o l / G l y c e r i n / F r u c t o s e / U r e a / C i t r i c Acid/Sodium Hydroxide/Maltose/Sodium PCA/Sodium Chloride/Sodium Lactate/Trehalose/Allantoin/Sodium Hyaluronate/Glucose, Trideceth-9/PEG-5 Isononanoate/Aqua, Glycereth-26, Fragrance (Parfum), Citric Acid, Methylcloroisothiazolinone/Methylisothiazolinone, Tetrasodium EDTA, Aqua/Betula Lenta Bark Oil/Vetiveria Zizanoides Root Oil/Linoleic Acid/Oleic Acid/Polysorbate 80/ Phenoxyethanol/Caprylyl Glycol/BHT.

DK12 Shower Gel Creamy

INGREDIENTS AND APPEARANCE

DK12 SHOWER GEL CREAMY 
benzalkonium chloride 0.13% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62476-010
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
ALLANTOIN (UNII: 344S277G0Z)
MALTOSE (UNII: XJ6S9RV06F)
GLYCERETH-26 (UNII: NNE56F2N14)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDE (UNII: 3BD22052MO)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
DISODIUM LAURYL SULFOSUCCINATE (UNII: P160Q81342)
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
UREA (UNII: 8W8T17847W)
TREHALOSE (UNII: B8WCK70T7I)
LAURETH-4 (UNII: 6HQ855798J)
COCAMIDE (UNII: 3YXD33R71G)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
EDETATE SODIUM (UNII: MP1J8420LU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
BETULA LENTA BARK (UNII: J689T0DVJQ)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM PIDOLATE (UNII: 1V74VH163T)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
FRUCTOSE (UNII: 6YSS42VSEV)
LINOLEIC ACID (UNII: 9KJL21T0QJ)
OLEIC ACID (UNII: 2UMI9U37CP)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
TRIDECETH-9 (UNII: X9HD79I514)
VETIVERIA ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62476-010-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/01/2023

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