CLOROX HEALTHCARE ALOEGUARD ANTIMICROBIAL- chloroxylenol liquid

Clorox HealthCare AloeGuard Antimicrobial by

Drug Labeling and Warnings

Clorox HealthCare AloeGuard 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

Chloroxylenol 0.75% w/w

Purpose

Antiseptic

Uses

• for hand-washing to decrease microbes on the skin
• ideal for daily repeated washings

Warnings

For external use only

WHEN USING

When using this product

• do not use in or near eyes
• discontue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• wet hands
• apply product (palmful)
• wash hands vigorously
• rinse thoroughly

Other information

• store at room temperatuure
• for healthcare professional use only

Inactive ingredients

Aloe Barbadensis Leaf Juice, Cocamide MEA, Coco-Betaine, Coconut Fatty Acid, D&C Green No. 8, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Glycerin, Hydroxypropyl Methylcellulose, Monoethanolamine, Oleic Acid, Propylene Glycol Sodium Sulfate, Tetrasodium EDTA, Water.

Package Label: 118ml/532ml/798ml/3785ml

CLOROX

HEALTHCARE

AloeGuard

Does Not Contain Bleach

Formerly

AloeGuard

from HealthLink

Antimcrobial Soap

INGREDIENTS AND APPEARANCE

CLOROX HEALTHCARE ALOEGUARD ANTIMICROBIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69540-0027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.75 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCO-BETAINE (UNII: 03DH2IZ3FY)
D&C GREEN NO. 8 (UNII: I2W85YOX9L)
OLEIC ACID (UNII: 2UMI9U37CP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM SULFATE (UNII: 0YPR65R21J)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
COCONUT ACID (UNII: 40U37V505D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MONOETHANOLAMINE (UNII: 5KV86114PT)
COCO MONOETHANOLAMIDE (UNII: C80684146D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69540-0027-1	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2021
2	NDC: 69540-0027-2	532 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2021
3	NDC: 69540-0027-4	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2021
4	NDC: 69540-0027-3	798 mL in 1 BAG; Type 0: Not a Combination Product	04/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2021

Labeler - Brand Buzz LLC (079266204)

Registrant - Brand Buzz LLC (079266204)