All Good Lavender Hand Sanitizer

Manufacturer
Bell International Laboratories, Inc
Effective date
2022-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:03:59

Label at a glance#

ProductAll Good Lavender Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Dispense an adequate amound in your palm to cover all surfaces of hands completely. Rub hands together until dry. Does not require rinsing.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire/flame.Do not use this product in or near eyes. If contact occurs rinse thoroughly with water. Keep out of reach of children. Children under six years of age should be supervised when using this product. In case of accidental ingestion, seek medical assistance or contact a poison control center immediately.

​

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children under six years of age should be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Dispense an adequate amound in your palm to cover all surfaces of hands completely. Rub hands together until dry. Does not require rinsing.

Other Information

OTHER SAFETY INFORMATION

Do not store above 104°C/40°F. May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Lavandula Latifolia Herb Oil, Thymus Vulgaris (Thyme) Leaf Extract, Tocopherol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-33776150-337-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
dc2c6420-1718-2e1e-e053-2995a90a259bdc2c6418-5036-1c2e-e053-2995a90aeb152022-04-08WarningsExact identifier
spl id: dc2c6420-1718-2e1e-e053-2995a90a259b
spl set id: dc2c6418-5036-1c2e-e053-2995a90aeb15

Reported adverse events (FAERS/openFDA)#

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