Reeva Green Apple Antibacterial Hand

Manufacturer: Abaco Partners LLC DBA Surefil
Effective date: 2019-10-16
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 00:07:04

Label at a glance#

ProductReeva Green Apple Antibacterial Hand

Active ingredientChloroxylenol

Label structure9 sections

Dosage and administration

Wash hands and rinse.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial Hand Soap

Use

INDICATIONS & USAGE SECTION

Helps fight germs on hands when used as a hand soap.

Warnings

WARNINGS SECTION

For External Use Only

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of eye contact, flush thoroughly with water. If swallowed, drink a glass of water to dilute. Call a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash hands and rinse.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sodium Lauryl Sulfate, Ethanol, Lauramine Oxide, Sodium Laureth Sulfate, Acrylic Polymer, Phenoxyethanol, Polypropylene Glycol 2000, PEG 8 Propylheptyl Ether, Sodium Chloride, Fragrance, MethyIisothiazolinone, FD&C Yellow #5, FD&C Blue #1.

SPL UNCLASSIFIED SECTION

Distributed by ALDI Inc.
Batavia, IL 60510

PRINCIPAL DISPLAY PANEL - 709 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REEVA_®

HAND
SOAP

ANTIBACTERIAL

green apple
POWERS AWAY
TOUGH FOODS!

ULTRA CONCENTRATED DISH DETERGENT

24 FL OZ
1.50 PT
709 mL

PRINCIPAL DISPLAY PANEL - 709 mL Bottle Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

Reeva Green Apple Antibacterial Hand
Chloroxylenol
WATER
SODIUM LAURYL SULFATE
ALCOHOL
LAURAMINE OXIDE
SODIUM LAURETH-3 SULFATE
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%)
PHENOXYETHANOL
PPG-26
DECETH-8
SODIUM CHLORIDE
METHYLISOTHIAZOLINONE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
20890-0091	20890-0091-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Chloroxylenol	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
ALCOHOL	3K9958V90M	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
SODIUM LAURETH-3 SULFATE	BPV390UAP0	IACT
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%)	M4PPW69Y4H	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
PPG-26	V86KZL3H2Z	IACT
DECETH-8	19FQ96EA8Q	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
551818c6-410d-48cf-9689-d5d255900de5			6f93aee4-3f2d-4cb9-9420-c01eeac1819c	2019-10-16	Warnings	Exact identifier spl id: 551818c6-410d-48cf-9689-d5d255900de5 spl set id: 6f93aee4-3f2d-4cb9-9420-c01eeac1819c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.