Plant Voice Hand Sanitizer

Manufacturer: Huizhou Bomei Cosmetic Co., Ltd.
Effective date: 2021-12-02
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 22:25:09

Label at a glance#

ProductPlant Voice Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antispetic

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteira on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flame
For external use only

When using this product

OTC - WHEN USING SECTION

Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
May discolor some fabrics.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

store below 105° F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide, Parfum (Fragrance), Aloe Barbadensis Leaf Extract.

Questions?

OTC - QUESTIONS SECTION

+86-752-5899111

Package Labeling: 72505-010-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label for 100mL

Package Labeling: 72505-010-50

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Plant Voice Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
PROPYLENE GLYCOL
SODIUM HYDROXIDE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72505-010	72505-010-10, 72505-010-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB

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
d23109a8-6e6a-bb57-e053-2a95a90a929d			f882455a-7bef-4cb2-a1cf-765ce19b0216	2021-12-02	Warnings	Exact identifier spl id: d23109a8-6e6a-bb57-e053-2a95a90a929d spl set id: f882455a-7bef-4cb2-a1cf-765ce19b0216

Reported adverse events (FAERS/openFDA)#

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