FDA.reportPublic FDA data

The Honest Company Hand Sanitizer Spray Orange Scent

Manufacturer
The Honest Company, Inc.
Effective date
2016-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:26:34

Label at a glance#

ProductHand Sanitizer Orange with aloe
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

Helps reduce bacteria on the skin Recommended for repeated use

Dosage and administration

Spray directly on hands and rub in thoroughly For children under 6, use adult supervision Not recommended for infants

Label contents#

Full prescribing information#

Active ingredient.....................Purpose

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%...............................Antiseptic

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire, sparks, and sources if ignition. Do not store above 104oF/40oC.

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 doctor if irritation and redness develop and persist for more than 72 hours

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

Warnings

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

  • Spray directly on hands and rub in thoroughly
  • For children under 6, use adult supervision
  • Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice, Glycerin, Citrus Aurantium Dulcis (Orange) Oil, Vanilla Planifolia Fruit Extract, Calendula Officinalis Flower Extract, Chamomilla Recutita Flower Extract, Triethyl Citrate

2 oz bottle label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 oz bottle label2 oz bottle label

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
69366-30169366-301-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
VANILLAQ74T35078HIACT
ALOE VERA LEAFZY81Z83H0XIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CHAMOMILEFGL3685T2XIACT
ORANGE OILAKN3KSD11BIACT
GLYCERINPDC6A3C0OXIACT
TRIETHYL CITRATE8Z96QXD6UMIACT

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
b9bf2dbd-d4f5-b7ea-e053-2995a90ae6ec33ac19ad-81cf-3ee3-e054-00144ff88e882021-01-25WarningsExact identifier
spl set id: 33ac19ad-81cf-3ee3-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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