FDA.reportPublic FDA data

Preface Earth Baby Hand Sanitizer Gel

Manufacturer
Earth Baby, Inc | V Manufacturing & Logistics, Inc.
Effective date
2020-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:43

Label at a glance#

ProductPreface Earth Baby Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other information do not store above 104°F (40°C).

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 62% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Uses to help reduce bacteria on the skin

DOSAGE & ADMINISTRATION SECTION

Directions apply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

STORAGE AND HANDLING SECTION

Other information do not store above 104°F (40°C).

INACTIVE INGREDIENT SECTION

Inactive ingredients Aloe Barbadensis Leaf Juice*, Carthamus Tinctorius (Safflower) Oleosomes*, Glycerin, Hydroxyethylcellulose, Helianthus Annuus (Sunflower) Seed Oil, Isopropyl Alcohol, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Parfum (Fragrance Natural), Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hyaluronate.

*Certified Organic Ingredient

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EBPHSG2EBPHSG2PEBHSG2DFPEBHSG2DF

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
62588-91462588-914-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UIACT
HYALURONATE SODIUMYSE9PPT4THIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
CARTHAMUS TINCTORIUS SEED OLEOSOMES9S60Q72309IACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
SUNFLOWER OIL3W1JG795YIIACT
ROSEMARYIJ67X351P9IACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
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
a3480ef9-0770-278b-e053-2995a90a4eb9a3481e29-2ca1-885e-e053-2995a90aba0b2020-04-14WarningsExact identifier
spl id: a3480ef9-0770-278b-e053-2995a90a4eb9
spl set id: a3481e29-2ca1-885e-e053-2995a90aba0b

Reported adverse events (FAERS/openFDA)#

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