FDA.reportPublic FDA data

Optimal Results Hand Sanitizer

Manufacturer
HB Media LLC (dba Optimal Results) | Fresh & Beautiful Cosmetics
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:53

Label at a glance#

ProductOptimal Results Hand Sanitizer
Active ingredientAlcohol
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For rinse-free hand sanitizing to remove 99.9% bacteria on skin.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other Information

OTHER SAFETY INFORMATION

Store under 105°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates Copolymer, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Principal Display Panel – Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MADE IN U.S.A.

HAND SANITIZER

KILLS 99.9% OF GERMS ON CONTACT

OPTIMAL RESULTS

ALCOHOL 70% TOPICAL GEL SOLUTION

  • ANTI-BACTERIAL
  • ANTI-VIRAL
  • CLEAN SCENT
  • WITH ALOE

8 Fl Oz (240 mL)

Principal Display Panel – Bottle Label
Principal Display Panel – Bottle Label

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
78956-101-012022-01-28C16284748780-1d6a99b39-8eba-a426-e053-dadaa90af4c2Drug Facts
78956-101-022022-01-28C16284748780-1d6a99b39-8eba-a426-e053-dadaa90af4c2Drug Facts
78956-101-032022-01-28C16284748780-1d6a99b39-8eba-a426-e053-dadaa90af4c2Drug Facts
78956-101-042022-01-28C16284748780-1d6a99b39-8eba-a426-e053-dadaa90af4c2Drug Facts
78956-101-052022-01-28C16284748780-1d6a99b39-8eba-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78956-101-01Optimal Results Hand Sanitizer240 mL in 1 BOTTLEGEL2401
78956-101-02Optimal Results Hand Sanitizer355 mL in 1 BOTTLEGEL3551
78956-101-03Optimal Results Hand Sanitizer500 mL in 1 BOTTLEGEL5001
78956-101-04Optimal Results Hand Sanitizer1000 mL in 1 BOTTLEGEL10001
78956-101-05Optimal Results Hand Sanitizer3785 mL in 1 BOTTLEGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78956-101OPTIMAL RESULTS HAND SANITIZER (ALCOHOL) GEL [HB MEDIA LLC (DBA OPTIMAL RESULTS)]1Legacy NDC, 5 package rows20200617_48218441-62a4-443a-ab4f-3700cb14591b.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
78956-10178956-101-01, 78956-101-02, 78956-101-03, 78956-101-04, 78956-101-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
Butyl Acrylate/Methyl Methacrylate/Methacrylic Acid Copolymer (18000 MW)JZ1374NL9EIACT
Aloe Vera LeafZY81Z83H0XIACT
GlycerinPDC6A3C0OXIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked)59TL3WG5COIACT
AminomethylpropanolLU49E6626QIACT

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
9e57e6ea-702e-40ea-b296-6bd6219fa37048218441-62a4-443a-ab4f-3700cb14591b2020-06-12WarningsExact identifier
spl id: 9e57e6ea-702e-40ea-b296-6bd6219fa370
spl set id: 48218441-62a4-443a-ab4f-3700cb14591b

Reported adverse events (FAERS/openFDA)#

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