Prince and Spring Moisturizing Hand Sanitizer

Manufacturer
Apollo Health and Beauty Care
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:22

Label at a glance#

ProductPrince and Spring Moisturizing Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For personal hand hygiene to help prevent the spread of bacterial, and can be used in place of hand washing if soap and water are not available.

Dosage and administration

For occasional and personal use Rub thoroughly into hands for at least 30 seconds. Allow to dry Children under 6 years should be supervised by an adult when using this product

Storage and handling

store at a temperature below 104°F (40°C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (65%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For personal hand hygiene to help prevent the spread of bacterial, and can be used in place of hand washing if soap and water are not available.

For external use only

WARNINGS SECTION

  • 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. Do not inhale or ingest.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds
  • on broken or damaged skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation 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

  • For occasional and personal use
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry
  • Children under 6 years should be supervised by an adult when using this product

Other Information

STORAGE AND HANDLING SECTION

  • store at a temperature below 104°F (40°C)
  • may discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-6, Fragrance, Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, AMP-Acrylates/Vinyl Isodecanoate Crosspolymer.

32 FL oz (946 ml)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP1PDP1

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
63148-528-322024-01-30C16284748780-11030e365-0941-111a-e063-dadaa90a10e2Prince and Spring Moisturizing Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-528-32Prince and Spring Moisturizing Hand Sanitizer946 mL in 1 BOTTLE, PLASTICGEL9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63148-528PRINCE AND SPRING MOISTURIZING HAND SANITIZER (ETHYL ALCOHOL) GEL [APOLLO HEALTH AND BEAUTY CARE]1Legacy NDC, 1 package rows20220105_d4c6649e-6af1-3cd8-e053-2a95a90af429.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-52863148-528-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
d4c66443-5e8a-1eba-e053-2995a90a5479d4c6649e-6af1-3cd8-e053-2a95a90af4292022-01-04WarningsExact identifier
spl id: d4c66443-5e8a-1eba-e053-2995a90a5479
spl set id: d4c6649e-6af1-3cd8-e053-2a95a90af429

Reported adverse events (FAERS/openFDA)#

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