PREMIER PURE PROTECTION

Manufacturer
RPP PRODUCTS, INC.
Effective date
2020-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:26

Label at a glance#

ProductPREMIER PURE PROTECTION
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Sanitizer to help reduce bacteria and germs on hands. For use when soap and water are not available.

Dosage and administration

Spray enough product to completly moisten and wipe clean until dry. children under 12 years of age should be supervised when using this PREMIER PURE

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Sanitizer to help reduce bacteria and germs on hands.

For use when soap and water are not available.

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 or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask doctor if

OTC - STOP USE SECTION

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 right away or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray enough product to completly moisten and wipe clean until dry.
  • children under 12 years of age should be supervised when using this PREMIER PURE

Other information

SPL UNCLASSIFIED SECTION

  • Store below 1100 F (430C)
  •  May discolor certain fabrics or surfaces 
  • This product does not contain any chemicals known to the State of California to cause cancer, birth defects, or any other reproductive harm

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerin, Tert-butyl Alcohol, Denatonium Benzoate

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73945-007-012022-01-28C16284748780-1d6a99b39-4bcb-a426-e053-dadaa90af4c2PREMIER PURE PROTECTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73945-007-01PREMIER PURE PROTECTION946 mL in 1 BOTTLE, PLASTICLIQUID9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73945-007PREMIER PURE PROTECTION (ALCOHOL 80%) LIQUID [RPP PRODUCTS, INC.]1Legacy NDC, 1 package rows20201202_01a8c339-edff-4a81-9020-0cc2a15c364b.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
73945-00773945-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
d21c3dde-58ea-48c0-ac41-3ca85552bc6501a8c339-edff-4a81-9020-0cc2a15c364b2020-11-23WarningsExact identifier
spl id: d21c3dde-58ea-48c0-ac41-3ca85552bc65
spl set id: 01a8c339-edff-4a81-9020-0cc2a15c364b

Reported adverse events (FAERS/openFDA)#

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