FDA.reportPublic FDA data

Hand Saniter Gel

Manufacturer
Alvachem LLC
Effective date
2020-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:35

Label at a glance#

ProductAlvaseptic
Active ingredientALCOHOL
Label structure8 sections

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

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.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat and flame.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water USP, Carbomer L, Triethanolamine, Diethanolamine, Monoethanolamine, Monoproplylene Glycol

When Using:

INDICATIONS & USAGE SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 73% V/V

1 gallon hand sanitizer gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alvaseptic Hand Sanitizing Gel Front Label 1 galAlvaseptic Hand Sanitizing Gel Front Label 1 galAlvaseptic Hand Sanitizing Gel Back Label 1 galAlvaseptic Hand Sanitizing Gel Back Label 1 gal

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
77312-01177312-011-15

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
DIETHANOLAMINEAZE05TDV2VIACT
TROLAMINE9O3K93S3TKIACT
MONOETHANOLAMINE5KV86114PTIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER TYPE C4Q93RCW27EIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
a7a917b1-a8c1-67ff-e053-2a95a90a4382a7a917b1-a8c0-67ff-e053-2a95a90a43822020-07-15WarningsExact identifier
spl id: a7a917b1-a8c1-67ff-e053-2a95a90a4382
spl set id: a7a917b1-a8c0-67ff-e053-2a95a90a4382

Reported adverse events (FAERS/openFDA)#

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