FDA.reportPublic FDA data

Sanitect Hand Sanitizer

Manufacturer
Aquagenics Technologies
Effective date
2023-07-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:28:07

Label at a glance#

ProductSanitect Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

Apply product onto hands, briskly rub hands together until dry without wiping. For children under 6, use only under adult supervision.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

OTC - STOP USE SECTION

Avoid contact with eyes. In case of contact, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.

OTC - STOP USE SECTION

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product onto hands, briskly rub hands together until dry without wiping. For children under 6, use only under adult supervision.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water, glycerin, carbomer, aloe.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFrontDrug FactsDrug Facts

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73763-465-012022-01-31C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-022022-01-31C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-032022-01-31C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-042022-01-31C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-052022-01-31C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-012022-01-28C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-022022-01-28C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-032022-01-28C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-042022-01-28C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b
73763-465-052022-01-28C16284748780-1d6a99b39-5994-a426-e053-dadaa90af4c2a16308a7-cc6d-b5ec-e053-2a95a90abd8b

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
73763-46573763-465-01, 73763-465-02, 73763-465-03, 73763-465-04, 73763-465-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT

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
28614340-46db-fac5-e063-6394a90a9156a16308a7-cc6d-b5ec-e053-2a95a90abd8b2024-12-03WarningsExact identifier
spl set id: a16308a7-cc6d-b5ec-e053-2a95a90abd8b

Reported adverse events (FAERS/openFDA)#

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