FDA.reportPublic FDA data

NDC- 63148-502, Guard Hand Sanitizer

Manufacturer
Apollo Health and Beauty Care
Effective date
2026-05-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:29

Label at a glance#

ProductGuard
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

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

Dosage and administration

For occassional and Personal use. Rub thoroughly into hands for at least 30 seconds. Allo to dry. Children under 6 years should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

  • Flammable
  • Keep away from source of heat or fire.

Do not use

OTC - DO NOT USE SECTION

  • On infants less than 2 months of age.
  • On open skin wounds
  • On broken or damaged skin.

When using this product avoid

OTC - WHEN USING SECTION

  • contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Do not inhale.

Stop use and ask a doctor

OTC - STOP USE SECTION

if 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 Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For occassional and Personal use.
  • Rub thoroughly into hands for at least 30 seconds. Allo to dry.
  • Children under 6 years should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), PEG-6, AMP-Acrylates/vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Isopropyl Alcohol, Isopropyl Myristate.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN5
581662ethanol 0.7 ML/ML Topical GelSCD5
581662ethanol 70 % Topical GelSY5
581662ethyl alcohol 70 % Topical GelSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-502-08Guard227 mL in 1 BOTTLE, PLASTICGEL2275

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63148-50263148-502-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT
POLYETHYLENE GLYCOL 3005655G9Y8AQIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ISOPROPYL ALCOHOLND2M416302IACT
ALOE VERA LEAFZY81Z83H0XIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
GuardALCOHOLApollo Health and Beauty Carefdc99948-1bd0-cdf2-e053-6394a90aaf972026-05-05WarningsExact identifier
ndc (package): 63148-502-08
ndc (product): 63148-502
ndc11 (package): 63148050208
spl id: 51162d81-5f65-c711-e063-6394a90aa33d
spl set id: fdc99948-1bd0-cdf2-e053-6394a90aaf97

Reported adverse events (FAERS/openFDA)#

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