FDA.reportPublic FDA data

PREMIUM HAND SANITIZER

Manufacturer
MD Science Lab LLC
Effective date
2020-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:22

Label at a glance#

ProductPREMIUM HAND SANITIZER
Active ingredientAlcohol
Label structure8 sections

Dosage and administration

Pump a small amount of liquid into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

  • For external use only.

OTC - WHEN USING SECTION

  • When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of liquid into palm of hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-6, AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Melaleuca Alternifolia (Tea Tree) Leaf Oil.

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

M.D.
Science Lab
LLC

PREMIUM
hand
sanitizer
with Tea Tree Oil & Aloe

Kills 99.99% of Germs
Antimicrobial

moisturizes & softens skin

3 fl oz 88ml℮

Principal Display Panel - 88 ml Bottle Label
Principal Display Panel - 88 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69898-601-012022-01-28C16284748780-1d6a99b39-efd8-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-601-032022-01-28C16284748780-1d6a99b39-efd8-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-601-082022-01-28C16284748780-1d6a99b39-efd8-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-601-122022-01-28C16284748780-1d6a99b39-efd8-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-601-322022-01-28C16284748780-1d6a99b39-efd8-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69898-601-01PREMIUM HAND SANITIZER3785 mL in 1 BOTTLE, PLASTICLIQUID37851
69898-601-03PREMIUM HAND SANITIZER88 mL in 1 BOTTLE, PLASTICLIQUID881
69898-601-08PREMIUM HAND SANITIZER236 mL in 1 BOTTLE, PLASTICLIQUID2361
69898-601-12PREMIUM HAND SANITIZER354 mL in 1 BOTTLE, PLASTICLIQUID3541
69898-601-32PREMIUM HAND SANITIZER946 mL in 1 BOTTLE, PLASTICLIQUID9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69898-601PREMIUM HAND SANITIZER (ALCOHOL) LIQUID [MD SCIENCE LAB LLC]1Legacy NDC, 5 package rows20200415_b7b35a4e-341d-41f5-96b4-01119a033159.zip

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
69898-60169898-601-03, 69898-601-08, 69898-601-12, 69898-601-32, 69898-601-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
POLYETHYLENE GLYCOL 3005655G9Y8AQIACT
Aloe Vera LeafZY81Z83H0XIACT
TEA TREE OILVIF565UC2GIACT

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
7c6f1a6d-e96c-445e-9b15-aeca4a205157b7b35a4e-341d-41f5-96b4-01119a0331592020-04-14WarningsExact identifier
spl id: 7c6f1a6d-e96c-445e-9b15-aeca4a205157
spl set id: b7b35a4e-341d-41f5-96b4-01119a033159

Reported adverse events (FAERS/openFDA)#

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