CLOROX ANTIMICROBIAL- benzalkonium chloride soap

Clorox Antimicrobial by

Drug Labeling and Warnings

Clorox Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Brand Buzz LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

• For handwashing to decrease bacteria on skin

Warnings

For external use only.

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water. If irritation persists, contact a Poison Control Center right away.

Keep out of reach of children.

Directions

• Apply onto wet hands, lather for 30 seconds and rinse thoroughly.

Other Information

• Avoid freezing and excessive heat above 40C (104F).

Inactive ingredients

Water, Sodium Laureth Sulfate, Sodium Chlroride, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Laureth-3, Sodium Bicarbonate, Disodium EDTA, Fragrance, Methylchloroisothiazolinone, Methylisothiazoline, Yellow 6(Ci 15985), Red 7(Ci 16255).

SPL UNCLASSIFIED SECTION

Do not add bleach.

Not for use in dishwashers.

PHOSPATE-FREE

BLEACH-FREE

Distributed by: Brand Buzz LLC., 1407 Broadway, New York, NY 10018

Clorox and logo are registered trademarks of the Clorox Company and are used under license by Brand Buzz LLC.
All Rights Reserved.

Questions or Comments?

Visit us at www.brandbuzzcp.com or call us at: 1-888-508-4750

For more product ingredient information, visit www.brandbuzzcp.com/ingredients

PRINCIPAL DISPLAY PANEL

Clorox

Antimicrobial

HandSoap

Ultra Concentrated Dishwashing Liquid

Orange Fusion

with Oxi

Bleach-Free

8FL OZ

(0.5 PT) 236 mL

Label

22FL OZ

(1.375 PT) 650 mL

INGREDIENTS AND APPEARANCE

CLOROX ANTIMICROBIAL 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69540-0030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
C12-14 PARETH-12 (UNII: M0LJS773XW)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
WATER (UNII: 059QF0KO0R)
PONCEAU 4R (UNII: Z525CBK9PG)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Characteristics
Color		Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69540-0030-1	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/2021
2	NDC: 69540-0030-2	650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2014

Labeler - Brand Buzz LLC (079266204)