P.O.V. Aloe Vera Hand Sanitizer

Manufacturer
Apollo Health and Beauty Care Inc.
Effective date
2018-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:56

Label at a glance#

ProductP.O.V. Aloe Vera Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

to help reduce bacteria on the skin.

Dosage and administration

put enough product in your palm to cover hands and rub hands together until dry. children under 6 years should be supervised when using this product.

Storage and handling

store at a temperature below 110°F (43°C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

  • flammable
  • keep away from source of heat or fire

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritaiton or redness develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • put enough product in your palm to cover hands and rub hands together until dry.
  • children under 6 years should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • store at a temperature below 110°F (43°C)
  • may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Fragrance (Parfum), Carbomber, Glycerin, Isopropyl Myristate, Isopropyl Alcohol, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Blue 1 (CI 42090), Yellow 5 (CI 19140).

Questions or comments?

OTC - QUESTIONS SECTION

1-866-695-3030

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the labelImage of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN1
902574ethanol 0.65 ML/ML Topical GelSCD1
902574ethyl alcohol 65 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63148-507-082024-01-30C16284748780-11030e365-16e6-111a-e063-dadaa90a10e258986197-5b97-4903-aaae-8f275e989f92

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-507-08P.O.V. Aloe Vera Hand Sanitizer237 mL in 1 BOTTLE, PLASTICGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63148-507P.O.V. ALOE VERA HAND SANITIZER (ETHYL ALCOHOL) GEL [APOLLO HEALTH AND BEAUTY CARE INC.]1Legacy NDC, 1 package rows20181010_58986197-5b97-4903-aaae-8f275e989f92.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-50763148-507-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
ca9eb55c-c0bb-4de5-92b1-c004ada952e058986197-5b97-4903-aaae-8f275e989f922018-10-09WarningsExact identifier
spl id: ca9eb55c-c0bb-4de5-92b1-c004ada952e0
spl set id: 58986197-5b97-4903-aaae-8f275e989f92

Reported adverse events (FAERS/openFDA)#

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