FDA.reportPublic FDA data

Advanced Hand Sanitizer

Manufacturer
Purchasing 411, Inc. | Blue Cross Laboratories, Inc
Effective date
2020-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:53

Label at a glance#

ProductAdvanced Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information do not store above 105ºF may discolor some fabrics harmful to wood finishes and plasics

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Use

  • To decrease bacteria on the skin that could cause disease.
  • recommended for repeated use

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.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if

  • Skin irritation develops

WARNINGS SECTION

Warnings

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

When using this product

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin
  • Do not inhale or ingest

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wet hands thoroughly with product and allow to dry without wiping
  • For children under 6, use only under adult supervision
  • not recommend for infants

STORAGE AND HANDLING SECTION

Other information

  • do not store above 105ºF
  • may discolor some fabrics
  • harmful to wood finishes and plasics

INACTIVE INGREDIENT SECTION

Inactive ingredients water, glycerin, propylene glycol,carbomer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Royalty Premier

Advanced

Hand Sanitizer

Fights Germs and Bacteria

40 FL OZ (1.18 L)

Royalty Premier Sanitizer backRoyalty Premier Sanitizer back

Royalty premier Sanitizer frontRoyalty premier Sanitizer front

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
79327-001-012022-01-28C16284748780-1d6a99b39-771d-a426-e053-dadaa90af4c2Advanced Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79327-001-01Advanced Hand Sanitizer1.18 L in 1 BOTTLEGEL1.181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79327-001ADVANCED HAND SANITIZER (ALCOHOL) GEL [PURCHASING 411, INC.]1Legacy NDC, 1 package rows20200719_aabb28bd-3634-db25-e053-2a95a90a4bb9.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79327-00179327-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
aabb3040-2fe6-bc0f-e053-2a95a90a8e47aabb28bd-3634-db25-e053-2a95a90a4bb92020-07-18WarningsExact identifier
spl id: aabb3040-2fe6-bc0f-e053-2a95a90a8e47
spl set id: aabb28bd-3634-db25-e053-2a95a90a4bb9

Reported adverse events (FAERS/openFDA)#

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