Energy Infusion Hand Sanitizer

Manufacturer: Landy International
Effective date: 2017-12-14
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 01:06:35

Label at a glance#

ProductEnergy Infusion Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

dosage

WARNINGS SECTION

warning

INACTIVE INGREDIENT SECTION

inactive

INDICATIONS & USAGE SECTION

indication

OTC - ACTIVE INGREDIENT SECTION

active

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keept out

OTC - PURPOSE SECTION

purpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51706-603-01	2024-06-13	C162847	48780-1	9d75b9d0-6ea4-f424-e053-dadaa90a57ce	604755c5-f2ee-3bbf-e053-2a91aa0a43cb
51706-603-01	2020-01-31	C162847	48780-1	9d75b9d0-6ea4-f424-e053-dadaa90a57ce	604755c5-f2ee-3bbf-e053-2a91aa0a43cb

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Energy Infusion Hand Sanitizer
Alcohol
EDETATE DISODIUM ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51706-603	51706-603-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1abdd6f7-3b46-09cc-e063-6394a90a7e71			604755c5-f2ee-3bbf-e053-2a91aa0a43cb	2024-06-13	Warnings	Exact identifier spl set id: 604755c5-f2ee-3bbf-e053-2a91aa0a43cb

Reported adverse events (FAERS/openFDA)#

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