FDA.reportPublic FDA data

VertecBio HS WB LSS

Manufacturer
Viking Chemical Co.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:17

Label at a glance#

ProductVertecBio HS WB LSS
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionsDirectionsPlace enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Warnings

WARNINGS SECTION

WarningsWarningsFor external use only. Flammable. Keep away from heat or flame.

Do not use: on children less than 2 months of age on open skin wounds

Uses

INDICATIONS & USAGE SECTION

UsesUsesHand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings - Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of childrenKeep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

OTC - PURPOSE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive IngredientsActive Ingretients Alcohol 66.2% w/w Purpose: Antiseptic

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredientsInactive ingredients ethyl lactate, glycerin, tocopheryl acetate, Klucel H CS, lime and sea salt fragrance

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug FactsDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74313-00174313-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)RFW2ET671PIACT
WATER059QF0KO0RIACT
ETHYL LACTATEF3P750VW8IIACT

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
d1f196a8-f5e9-ccaa-e053-2a95a90a844ca79981d4-c1ac-e58a-e053-2a95a90a12472021-11-29WarningsExact identifier
spl set id: a79981d4-c1ac-e58a-e053-2a95a90a1247

Reported adverse events (FAERS/openFDA)#

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