FDA.reportPublic FDA data

Sanitizing Wipes Grapefruit

Manufacturer
The Honest Company Inc.
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:54:43

Label at a glance#

ProductSanitizing Wipes Grapefruit
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 65%

DOSAGE & ADMINISTRATION SECTION

Directions

• Wipe hands thoroughly with product when there’s no soap and water around. Discard after use, please don’t flush.

• For children under 6, use adult supervision

INACTIVE INGREDIENT SECTION

Inactive ingredients

  • Water, Glycerin, Triethyl Citrate, Citrus Paradisi (Grapefruit) Peel Oil, Aloe Barbadensis Leaf Extract, Gamma-Undecalactone, Methylbenzyl Acetate, Neral, Ethyl Hydroxypyrone, Ethyl Butyrate, Furaneol, Grapefruit Mercaptan, Limonene

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

• Helps reduce bacteria on the skin.

• Recommended for repeated use.

OTHER SAFETY INFORMATION

Other Safety Information

• Do not use as a baby wipe

• Do not use in genital area or on damaged skin

WARNINGS SECTION

Warnings

  • For external use only
  • Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104°F/40°C

OTC - WHEN USING SECTION

When using this product

• Keep out of eyes

• In case of contact with eyes, flush thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanitizing Wipes Grapefruit 15 ctSanitizing Wipes Grapefruit 15 ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanitizing Wipes Grapefruit 50ctSanitizing Wipes Grapefruit 50ct

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
884787ethanol 65 % Medicated PadPSN2
884787ethanol 0.65 ML/ML Medicated PadSCD2
884787ethanol 65 % Medicated PadSY2
884787ethyl alcohol 65 % WipesSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69366-320-24Sanitizing Wipes Grapefruit50 mL in 1 POUCHCLOTH502
69366-320-25Sanitizing Wipes Grapefruit3 in 1 PACKAGECLOTH32
69366-320-26Sanitizing Wipes Grapefruit15 mL in 1 POUCHCLOTH152

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
69366-32069366-320-24, 69366-320-26, 69366-320-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
METHYLBENZYL ACETATEP4RVP859F5IACT
CITRALT7EU0O9VPPIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
GLYCERINPDC6A3C0OXIACT
GAMMA-UNDECALACTONEQB1T0AG2YLIACT
LIMONENE, (+)-GFD7C86Q1WIACT
CITRUS PARADISI (GRAPEFRUIT) PEEL OILYR377U58W9IACT
WATER059QF0KO0RIACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
ETHYL BUTYRATEUFD2LZ005DIACT
ETHYL HYDROXYPYRONEL6Q8K29L05IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-02-12monthly-update2026-06-03 17:56:27

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
Sanitizing Wipes GrapefruitALCOHOLThe Honest Company Inc.4aa8c899-e5c3-9eec-e063-6294a90a6eae2026-04-22WarningsExact identifier
ndc (package): 69366-320-25
ndc (package): 69366-320-26
ndc (package): 69366-320-24
ndc (product): 69366-320
ndc11 (package): 69366032026
ndc11 (package): 69366032024
ndc11 (package): 69366032025
spl id: 50127b07-9818-7911-e063-6394a90a9940
spl set id: 4aa8c899-e5c3-9eec-e063-6294a90a6eae

Reported adverse events (FAERS/openFDA)#

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