FDA.reportPublic FDA data

Hand Sanitizer Gel

Manufacturer
NV Labs
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:42

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

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

Dosage and administration

Directions Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Ethyl Alcohol 70% v/v Antimicrobial

USES

INDICATIONS & USAGE SECTION

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

WARNING

WARNINGS SECTION

Warnings

Flammable Keep away from Flame

For External Use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appeara and lasts

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using this product

Other information

OTHER SAFETY INFORMATION

Other Information

  • Store below 110F (43C) May discolor certain fabrics or surfaces

In active Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua) , Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Tocopheryl Acetate, Carbomer, Triethanolamine, Fragrance (Parfum)

Manufactured By: Questions or Comments

OTC - QUESTIONS SECTION

Manufactured By: Reforma Group, Southfield, Michigan 48033

Questions or comments? Call 1-248-358-9022

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

Antimicrobial

PRINCIPLE DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front of LabelFront of LabelBack of LabelBack of LabelAmber and Black

HAND SANITIZER GEL

MADE IN USA

NDC 73696-102-04

KILLS 99.99% of Germs

4 fl. oz (120 mL)

Amber and Black

HAND SANITIZER GEL

MADE IN USA

NDC 73696-102-16

KILLS 99.99% of Germs

16 fl.oz (473 mL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73696-102-042024-01-30C16284748780-11030e365-36c3-111a-e063-dadaa90a10e2Amber and Black HAND SANITIZER GEL (4 Fl. Oz & 16 Fl Oz.)
73696-102-162024-01-30C16284748780-11030e365-36c3-111a-e063-dadaa90a10e2Amber and Black HAND SANITIZER GEL (4 Fl. Oz & 16 Fl Oz.)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73696-102-04Hand Sanitizer Gel120 mL in 1 BOTTLE, PLASTICGEL1202
73696-102-16Hand Sanitizer Gel473 mL in 1 BOTTLE, PLASTICGEL4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73696-102HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [NV LABS]2Legacy NDC, 2 package rows20220114_a19ef496-9624-fea7-e053-2a95a90a7091.zip

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
73696-10273696-102-04, 73696-102-16

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
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT

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
d57887f1-ddfb-1fa4-e053-2995a90a9e35a19ef496-9624-fea7-e053-2a95a90a70912022-01-13WarningsExact identifier
spl id: d57887f1-ddfb-1fa4-e053-2995a90a9e35
spl set id: a19ef496-9624-fea7-e053-2a95a90a7091

Reported adverse events (FAERS/openFDA)#

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