FDA.reportPublic FDA data

BM013 Plant Voice Hand Sanitizer

Manufacturer
Huizhou Bomei Cosmetic Co., Ltd.
Effective date
2020-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:20:36

Label at a glance#

ProductBM013 Plant Voice Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria 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

+1-315-636-0065

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72505-02272505-022-30

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
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d23f16b5-64e0-1dac-e053-2a95a90aa4c4df44564a-38f3-4468-a6c1-0b63ff53532b2021-12-03WarningsExact identifier
spl set id: df44564a-38f3-4468-a6c1-0b63ff53532b

Reported adverse events (FAERS/openFDA)#

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