HUSTLE BUBBLES DELUXE- benzalkonium chloride soap

HUSTLE BUBBLES DELUXE by

Drug Labeling and Warnings

HUSTLE BUBBLES DELUXE by is a Otc medication manufactured, distributed, or labeled by H.B.D. DIST. INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS:

Active Ingredient:

Benzalkonium Chloride 0.10%

PURPOSE

Antimicrobial

USES:

An effective antimicrobial skin cleanser. For use as a wash to decrease bacteria on skin, all while gently cleaning, soothing and nourishing.

Reduces possibility of cross contamination.   

WARNINGS

WARNING: FOR EXTERNAL USE ONLY
WHEN USING THIS PRODUCT:
DO NOT USE NEAR OR IN THE EYES
AVOID IF ALLERGIC TO INGREDIENTS

KEEP OUT OF REACH OF CHILDREN

KEEP AWAY FROM CHILDREN. If swallowed, get medical attention & contact a POISON CONTROL CENTER immediately.

DOSAGE & ADMINISTRATION

DIRECTIONS: Use to replace green-soap and in-process washes.

Use to keep fresh tattoos clean during the healing process.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Aloe Barbadensis (Aloe Vera) Leaf Extract, Soytrimonium Chloride (and) Propylene Glycol, Coceth- 7 (and) PPG-1-PEG-9 Lauryl Glycol Ether (and) PEG-40 Hydrogenated Castor Oil, Rosmarinus Officinalis (Rosemary Cineole) Oil, Camellia Oleifera (Japanese Green Tea) Leaf Extract, Arnica Montana Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Hamamelis Virginiana (Witch Hazel) Extract, Symphytum Officinale (Comfrey) Leaf Extract, Methylchloroisothiazolinone & Methylisothiazolinone

QUESTIONS

QUESTIONS: 718-352-4705 (M-F, 9-5 EST) or www.hustlebutter.com

SPL UNCLASSIFIED SECTION

REVOLUTIONARY REFINED RINSE

Antimicrobial Foam Soap Soft & Gentle

YOU CAN'T KNOCK THE HUSTLE®

Cruelty Free

Made With Natural Ingredients

Made in the U.S.A and Distributed by:

H.B.D. DIST. INC.
Franklin Square, NY 11010

Imported to the EU by

Killer Ink Ltd.

54 Evans Road, Venture Point, Speke, Liverpool L24 9PB U.K.

Packaging

INGREDIENTS AND APPEARANCE

HUSTLE BUBBLES DELUXE 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72014-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TRIMETHYLAMINE HYDROCHLORIDE (UNII: UW38SRM77K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCETH-7 (UNII: 58Y261JLH5)
PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
ROSEMARY OIL (UNII: 8LGU7VM393)
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CHAMOMILE (UNII: FGL3685T2X)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
COMFREY LEAF (UNII: DG4F8T839X)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72014-100-07	207 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/13/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/13/2018

Labeler - H.B.D. DIST. INC. (031127044)