FDA.reportPublic FDA data

INSTANT HAND SANITIZER

Manufacturer
APOLLO HEALTH AND BEAUTY CARE
Effective date
2010-07-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:00

Label at a glance#

ProductINSTANT HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E
Active ingredientALCOHOL
Label structure5 sections

Indications and uses

USES: TO HELP REDUCE BACTERIA ON THE SKIN. DIRECTIONS: APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

Dosage and administration

USES: TO HELP REDUCE BACTERIA ON THE SKIN. DIRECTIONS: APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

Storage and handling

DO NOT STORE ABOVE 110 0 F (43 0 C). MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62% (ANTISEPTIC)

USES AND DIRECTIONS

OTC - PURPOSE SECTION

  • USES: TO HELP REDUCE BACTERIA ON THE SKIN.
  • DIRECTIONS: APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

WARNINGS

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.FLAMMABLE KEEP AWAY FROM FIRE OR FLAME.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

  • IRRITATION OR RASH DEVELOPS 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.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

DO NOT STORE ABOVE 1100F (430C). MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

PACKAGE FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

  • 15OZ FRONT AND BACK LABELS: care15.jpg15OZ FRONT AND BACK LABELS15OZ FRONT AND BACK LABELS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63148-225-152020-01-31C16284748780-19d75b9d1-0cc3-f424-e053-dadaa90a57ceBACK LABEL - DRUG FACTS BOX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-225-15INSTANT HAND SANITIZERWITH MOISTURIZERS AND VITAMIN E443 mL in 1 BOTTLE, PUMPGEL4431

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63148-225INSTANT HAND SANITIZER WITH MOISTURIZERS AND VITAMIN E (ETHYL ALCOHOL) GEL [APOLLO HEALTH AND BEAUTY CARE]1Legacy NDC, 1 package rows20100706_40f48b3f-5ba8-40e6-85b1-3565f8607e48.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-22563148-225-15

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB

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
7fee5284-8e16-4511-8e94-daf556137e7f40f48b3f-5ba8-40e6-85b1-3565f8607e482010-07-05WarningsExact identifier
spl id: 7fee5284-8e16-4511-8e94-daf556137e7f
spl set id: 40f48b3f-5ba8-40e6-85b1-3565f8607e48

Reported adverse events (FAERS/openFDA)#

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