Antibacterial Hand Sanitizer

Manufacturer
TEKWELD SOLUTIONS, INC.
Effective date
2024-12-03
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 00:40:15

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Wet hands throughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings Flammable.

WARNINGS SECTION

Keep away from fire or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, rinse with water.

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly and contact Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands throughly with product and allow to dry without wiping.

Other Information

SPL UNCLASSIFIED SECTION

Store under 105°F.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbomer,Fragrance,Glycerin,Propylene Glycol, Tocopheryl Acetate,Triethanolamine,Water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label059Label059

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label029Label029

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label15Label15

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label30Label30

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label58Label58

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label60Label60

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN11
581660ethanol 0.62 ML/ML Topical GelSCD11
581660ethanol 62 % Topical GelSY11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71160-180-15Antibacterial Hand Sanitizer15 mL in 1 BOTTLEGEL1511
71160-180-29Antibacterial Hand Sanitizer29 mL in 1 BOTTLEGEL2911
71160-180-30Antibacterial Hand Sanitizer30 mL in 1 BOTTLEGEL3011
71160-180-53Antibacterial Hand Sanitizer53 mL in 1 BOTTLEGEL5311
71160-180-58Antibacterial Hand Sanitizer58 mL in 1 BOTTLEGEL5811
71160-180-59Antibacterial Hand Sanitizer59 mL in 1 BOTTLEGEL5911
71160-180-60Antibacterial Hand Sanitizer60 mL in 1 BOTTLEGEL6011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71160-180ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [TEKWELD SOLUTIONS, INC.]11Current NDC, Legacy NDC, 7 package rows20241205_45afc52b-9838-1729-e054-00144ff8d46c.zip

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
71160-18071160-180-59, 71160-180-29, 71160-180-15, 71160-180-30, 71160-180-58, 71160-180-60, 71160-180-53

Ingredients#

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

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

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
Antibacterial Hand SanitizerALCOHOLTEKWELD SOLUTIONS, INC.45afc52b-9838-1729-e054-00144ff8d46c2024-12-03WarningsExact identifier
ndc (package): 71160-180-29
ndc (package): 71160-180-53
ndc (package): 71160-180-58
ndc (package): 71160-180-15
ndc (package): 71160-180-60
ndc (package): 71160-180-30
ndc (package): 71160-180-59
ndc (product): 71160-180
ndc11 (package): 71160018015
ndc11 (package): 71160018030
ndc11 (package): 71160018058
ndc11 (package): 71160018059
ndc11 (package): 71160018053
ndc11 (package): 71160018060
ndc11 (package): 71160018029
spl id: 285edb29-9a5c-40ee-e063-6394a90adabb
spl set id: 45afc52b-9838-1729-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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