Grove Hand Sanitizer Spray Blood Orange

Manufacturer
Bell International Laboratories
Effective date
2020-04-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:24

Label at a glance#

ProductGrove Blood Orange
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

Helps decrease bacteria on skin. Recommended for repeated use.

Dosage and administration

Shake well. Spray onto palms and rub thoroughly. For children under 6 years, use adult supervision. Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps decrease bacteria on skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable keep away from fire or flame

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin

Stop use and ask a docutor if irritation or redness develop and persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well. Spray onto palms and rub thoroughly. For children under 6 years, use adult supervision. Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Orange (Citrus Aurantium Dulcis) Oil, Glycerin, Aloe Vera (Aloe Barbadensis) Leaf Juice, Coconut (Cocos Nucifera) Oil, Sunflower (Helianthus Annuus) Seed Oil, Jojoba (Simmondsia Chinensis) Seed Oil, Tocopheryl Acetate

2 oz spray label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

outsideoutsideinsideinside

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76150-236-412023-01-30C16284748780-1f386c649-ad42-0266-e053-dadaa90a7c1aGrove Hand Sanitizer Spray Blood Orange

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
76150-23676150-236-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a368d56b-661a-78f7-e053-2a95a90a8945a368d56b-6619-78f7-e053-2a95a90a89452020-04-16WarningsExact identifier
spl id: a368d56b-661a-78f7-e053-2a95a90a8945
spl set id: a368d56b-6619-78f7-e053-2a95a90a8945

Reported adverse events (FAERS/openFDA)#

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