FDA.reportPublic FDA data

Sanitex MVP Foam Anti-Bacterial

Manufacturer
Vectair Systems, Inc.
Effective date
2018-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:41:39

Label at a glance#

ProductSanitex MVP Foam Anti-Bacterial
Active ingredientCHLOROXYLENOL
Label structure7 sections

Dosage and administration

Wet hands and forearms. Apply a palmful to hands & forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely & dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.75%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial  

Use

INDICATIONS & USAGE SECTION

Reduces amount of bacteria on hands

Warnings

WARNINGS SECTION

For external use only.  Do not use in eyes.

Discontinue use if irritation & redness develop.  If condition persists for more than 72 hours, consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Not for use on children under six months of age.

For institutional & professional use only.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and forearms.
  • Apply a palmful to hands & forearms.
  • Scrub thoroughly for at least fifteen seconds.
  • Rinse completely & dry.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, TEA-Lauryl Sulfate, Lauramide DEA, Fragrance, DMDM Hydantoin, Yellow 5, Blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 x 1000 mL Label4 x 1000 mL Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52007-40052007-400-04, 52007-400-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TRIETHANOLAMINE LAURYL SULFATEE8458C1KAAIACT
LAURIC DIETHANOLAMIDEI29I2VHG38IACT
DMDM HYDANTOINBYR0546TOWIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
c922f01e-c430-4b20-bcc0-0ca233a4d88e41848005-ac76-4a06-a70b-5d882762fdbe2018-12-14WarningsExact identifier
spl id: c922f01e-c430-4b20-bcc0-0ca233a4d88e
spl set id: 41848005-ac76-4a06-a70b-5d882762fdbe

Reported adverse events (FAERS/openFDA)#

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