Health N Hygiene Hand Sanitizer

Manufacturer
Sai N.M. Ventures LLC
Effective date
2020-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:33

Label at a glance#

ProductHealth N Hygiene Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using sanitizer.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose:

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to reduce bacteria on the skin that could cause disease.

Recommended for repeated use.

Warning:

WARNINGS SECTION

Flammable. Keep away from fire or flames.

When using this product 

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash appears and lasts 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using sanitizer.

Other Information:

SPL UNCLASSIFIED SECTION

Store below 110 °F (43°C)

May discolor certain fabrics or surfaces 

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water(Aqua), Carbomer, Glycerin, Propylene Glycol.

Package Labeling:60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:120ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80198-001-002022-01-28C16284748780-1d6a99b39-b688-a426-e053-dadaa90af4c2Health N Hygiene Hand Sanitizer
80198-001-012022-01-28C16284748780-1d6a99b39-b688-a426-e053-dadaa90af4c2Health N Hygiene Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80198-001-00Health N Hygiene Hand Sanitizer60 mL in 1 BOTTLEGEL601
80198-001-01Health N Hygiene Hand Sanitizer120 mL in 1 BOTTLEGEL1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80198-001HEALTH N HYGIENE HAND SANITIZER (ALCOHOL) GEL [SAI N.M. VENTURES LLC]1Legacy NDC, 2 package rows20201014_b09cbfcd-fbcf-d7a8-e053-2995a90ad197.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80198-00180198-001-00, 80198-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b09cb8d5-8ea2-5bd1-e053-2995a90ab7cab09cbfcd-fbcf-d7a8-e053-2995a90ad1972020-10-01WarningsExact identifier
spl id: b09cb8d5-8ea2-5bd1-e053-2995a90ab7ca
spl set id: b09cbfcd-fbcf-d7a8-e053-2995a90ad197

Reported adverse events (FAERS/openFDA)#

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