HDX Hand Sanitizer

Manufacturer
Apollo Health and Beauty Care
Effective date
2016-08-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:52

Label at a glance#

ProductHDX Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Put enough hand sanitizer 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 70% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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

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

  • Put enough hand sanitizer 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), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Propylene Glycol, Glycerin, Isopropyl Myristate, Tocopheryl  Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Ethylhexylglycerin, Yellow 5 (CI 19140), Blue 1 (CI 42090).

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the 8oz labelImage of the 8oz label

Image of the 2oz labelImage of the 2oz label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63148-479-022024-01-30C16284748780-11030e365-35f8-111a-e063-dadaa90a10e2DRUG FACTS
63148-479-082024-01-30C16284748780-11030e365-35f8-111a-e063-dadaa90a10e2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-479-02HDX Hand Sanitizer59 mL in 1 BOTTLE, PLASTICLIQUID591
63148-479-08HDX Hand Sanitizer236 mL in 1 BOTTLE, PLASTICLIQUID2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63148-479HDX HAND SANITIZER (ETHYL ALCOHOL) LIQUID [APOLLO HEALTH AND BEAUTY CARE]1Legacy NDC, 2 package rows20160823_699b46e4-d352-4bf5-bef5-6f108f7e078f.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-47963148-479-08, 63148-479-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
8a83e36a-2186-4518-b0ea-7c67c1c96800699b46e4-d352-4bf5-bef5-6f108f7e078f2016-08-22WarningsExact identifier
spl id: 8a83e36a-2186-4518-b0ea-7c67c1c96800
spl set id: 699b46e4-d352-4bf5-bef5-6f108f7e078f

Reported adverse events (FAERS/openFDA)#

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