FDA.reportPublic FDA data

PREMIUM HAND SANITIZER

Manufacturer
MD Science Lab LLC
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:35

Label at a glance#

ProductPREMIUM HAND SANITIZER
Active ingredientAlcohol
Label structure8 sections

Dosage and administration

Dispense a small amount 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 80%

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

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerin, Hydrogen Peroxide.

PRINCIPAL DISPLAY PANEL - 3.7 liter Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

M.D.
Science Lab
LLC

PREMIUM
hand
sanitizer

Kills 99.99% of Germs

moisturizes & softens skin

1 gal 128 fl oz 3.7 liter e

PRINCIPAL DISPLAY PANEL - 3.7 liter Bottle Label
PRINCIPAL DISPLAY PANEL - 3.7 liter Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN1
1041498ethanol 0.8 ML/ML Topical GelSCD1
1041498ethanol 80 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69898-801-012022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-032022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-082022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-122022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-162022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-272022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-322022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER
69898-801-552022-01-28C16284748780-1d6a99b39-760c-a426-e053-dadaa90af4c2PREMIUM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69898-801-01PREMIUM HAND SANITIZER3785 mL in 1 BOTTLE, PLASTICLIQUID37851
69898-801-03PREMIUM HAND SANITIZER88 mL in 1 BOTTLE, PLASTICLIQUID881
69898-801-08PREMIUM HAND SANITIZER236 mL in 1 BOTTLE, PLASTICLIQUID2361
69898-801-12PREMIUM HAND SANITIZER354 mL in 1 BOTTLE, PLASTICLIQUID3541
69898-801-16PREMIUM HAND SANITIZER473 mL in 1 BOTTLE, PLASTICLIQUID4731
69898-801-27PREMIUM HAND SANITIZER1040988 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID10409881
69898-801-32PREMIUM HAND SANITIZER946 mL in 1 BOTTLE, PLASTICLIQUID9461
69898-801-55PREMIUM HAND SANITIZER208197 mL in 1 DRUMLIQUID2081971

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69898-801PREMIUM HAND SANITIZER (ALCOHOL) LIQUID [MD SCIENCE LAB LLC]1Legacy NDC, 8 package rows20200701_32d8c570-3d77-4d18-883f-da7ed3ae65bc.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69898-80169898-801-03, 69898-801-08, 69898-801-12, 69898-801-32, 69898-801-01, 69898-801-55, 69898-801-27, 69898-801-16

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
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT
POLYETHYLENE GLYCOL 3005655G9Y8AQIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
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
3350ca88-187a-4ea3-94b9-4211bec5e52132d8c570-3d77-4d18-883f-da7ed3ae65bc2020-06-29WarningsExact identifier
spl id: 3350ca88-187a-4ea3-94b9-4211bec5e521
spl set id: 32d8c570-3d77-4d18-883f-da7ed3ae65bc

Reported adverse events (FAERS/openFDA)#

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