FDA.reportPublic FDA data

Purcol Moisturizing Hand Sanitizer

Manufacturer
Purocol LLC
Effective date
2022-03-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:34

Label at a glance#

ProductPurcol Moisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together until dry No rinsing required No towels needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease
  • Recommended for repeated use

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 a 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 or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together until dry
  • No rinsing required
  • No towels needed

Other Information

SPL UNCLASSIFIED SECTION

  • Store below 104°F (40°C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Barbadensis Leaf Extract, Hydroxypropyl cellulose, Lauryl lactate, Myristyl lactate, Cetyl lactate, Fragrance.

Package Labeling:60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:251.3ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:473.1ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75266-685-602024-01-30C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-612024-01-30C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-622024-01-30C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-602022-03-01C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-612022-03-01C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-622022-03-01C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-602022-01-28C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-612022-01-28C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer
75266-685-622022-01-28C16284748780-1d6a99b39-a60a-a426-e053-dadaa90af4c2Purcol Moisturizing Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75266-685-60Purcol Moisturizing Hand Sanitizer60 mL in 1 TUBEGEL602
75266-685-61Purcol Moisturizing Hand Sanitizer251.3 mL in 1 BOTTLEGEL251.32
75266-685-62Purcol Moisturizing Hand Sanitizer473.1 mL in 1 BOTTLEGEL473.12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75266-685PURCOL MOISTURIZING HAND SANITIZER (ALCOHOL) GEL [PUROCOL LLC]2Legacy NDC, 3 package rows20220302_a592acd5-b6d7-7981-e053-2a95a90a0448.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
75266-68575266-685-60, 75266-685-61, 75266-685-62

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
LAURYL LACTATEG5SU0BFK7OIACT
MYRISTYL LACTATE1D822OC34XIACT
CETYL LACTATEA7EVH2RK4OIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
d92db1de-7a64-c541-e053-2a95a90a37e1a592acd5-b6d7-7981-e053-2a95a90a04482022-03-01WarningsExact identifier
spl id: d92db1de-7a64-c541-e053-2a95a90a37e1
spl set id: a592acd5-b6d7-7981-e053-2a95a90a0448

Reported adverse events (FAERS/openFDA)#

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