FDA.reportPublic FDA data

Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil

Manufacturer
TJA Health LLC
Effective date
2023-12-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:17:09

Label at a glance#

ProductCoconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

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

Dosage and administration

Apply to dry hands, rub together, & let dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

USES

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only. Avoid contact with eyes. In case of eye contact, flush with water. Discontinue use if irritation or redness occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

2 years of age and younger. If swallowed, get help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply to dry hands, rub together, & let dry.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified water, surfactant, vitamin E(natural, d-alpha tocopherol), almond oil (natural), polysorbate 20, isopropyl alcohol USP, natural essential oil complex, natutal coconut scent.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57660-004-012025-02-03C16284748780-12cef2736-7d98-d83d-e063-dadaa90ab31fCoconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil
57660-004-012025-01-30C16284748780-12cef2736-7d98-d83d-e063-dadaa90ab31fCoconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57660-00457660-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALMOND OIL66YXD4DKO9IACT
POLYSORBATE 207T1F30V5YHIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
ACETAMIDOETHOXYETHANOLLVX2APC4XRIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT

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
2d3fe528-a52a-ca3a-e063-6394a90a8452ef421e7b-01ac-4ee6-b96f-a2fa476741b02025-02-03WarningsExact identifier
spl set id: ef421e7b-01ac-4ee6-b96f-a2fa476741b0

Reported adverse events (FAERS/openFDA)#

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