FDA.reportPublic FDA data

33.8oz SaniPure Hand Sanitizer with Aloe Vera and Vitamin E

Manufacturer
FLPHARMACEUTICALS LLC
Effective date
2020-05-08
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 23:32:00

Label at a glance#

Product33.8oz SaniPure Hand Sanitizer with Aloe Vera and Vitamin E
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Wet hands thoroughly with product. Briskly rub hands together until dry. Supervise children under 6 years in the use of this product. SaniPure .

Label contents#

Full prescribing information#

Kills 99% of Germs

INDICATIONS & USAGE SECTION

SaniPure allows you to wash your hands whenever conventional soap and water is not available. Use as an aid to reduce exposure to infectious germs and to supplement daily handwashing. Helps meet U.S. Government standards by protecting against exposure to bloodborne diseases. Nontozic-For External Use Only.

Keep bottle of SaniPure in

  • Kitchen Medical Offices Nurseries
  • Automobile Bathrooms Workplace

Drug Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product. Briskly rub hands together until dry.
  • Supervise children under 6 years in the use of this product. SaniPure.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Aloe Vera, Carbomer, Fragrance, Glycerin, Vitamin E, Triethanolamine.

Warning

WARNINGS SECTION

  • Flammable, keep away from flame.
  • Keep out of eyes. In case of eye contact immediately flush eyes with water then contact physician.
  • If swallowed, contact physician.
  • For External Use Only.
  • Do not store above 110℉。

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71724-500-982022-11-17C16284748780-1c7ccaba7-2988-fd44-e053-dadaa90aa01b72bccf99-635e-41cb-b85d-bd6d28e9ddcf
71724-500-992022-11-17C16284748780-1c7ccaba7-2988-fd44-e053-dadaa90aa01b72bccf99-635e-41cb-b85d-bd6d28e9ddcf
71724-500-982021-07-23C16284748780-1c7ccaba7-2988-fd44-e053-dadaa90aa01b72bccf99-635e-41cb-b85d-bd6d28e9ddcf
71724-500-992021-07-23C16284748780-1c7ccaba7-2988-fd44-e053-dadaa90aa01b72bccf99-635e-41cb-b85d-bd6d28e9ddcf

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71724-50071724-500-98, 71724-500-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA WHOLEKIZ4X2EHYXIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
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
ed88620e-e0a5-c2cb-e053-2a95a90a327b72bccf99-635e-41cb-b85d-bd6d28e9ddcf2022-11-15WarningsExact identifier
spl set id: 72bccf99-635e-41cb-b85d-bd6d28e9ddcf

Reported adverse events (FAERS/openFDA)#

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