FDA.reportPublic FDA data

BELLI MOISTURIZING HAND SANITIZER

Manufacturer
ABT Belli-Materna Inc
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:46:28

Label at a glance#

ProductBELLI MOISTURIZING HAND SANITIZER 0.1 PERCENT
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

REDUCES BACTERIA ON THE SKIN

Dosage and administration

PLACE ENOUGH PRODUCT IN YOUR HANDS TO THOROUGHLY COVER YOUR HANDS AND RUB IN.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USES

INDICATIONS & USAGE SECTION

  • REDUCES BACTERIA ON THE SKIN

WARNINGS

WARNINGS SECTION

WHEN USING THIS PRODUCT

  • KEEP OUT OF EYES / RINSE WITH WATER TO REMOVE

STOP USE AND ASK A DOCTOR IF

  • RASH OR SKIN ORRITATION DEVELOPS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

IN CASE OF ACCIDENTAL INGESTION, CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • PLACE ENOUGH PRODUCT IN YOUR HANDS TO THOROUGHLY COVER YOUR HANDS AND RUB IN.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, SD ALCOHOL 40-B, POLYSORBATE 20, PEG-7 GLYCERYL COCOATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE, CITRUS LIMON (LEMON) PEEL OIL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hand Sanitizer 2oz01b LBL_Hand Sanitizer 2oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1102185benzalkonium chloride 0.1 % Topical LotionPSN8
1102185benzalkonium chloride 1 MG/ML Topical LotionSCD8
1102185benzalkonium chloride 0.1 % Topical LotionSY8

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42281-101-112024-01-30C16284748780-11030e365-6dff-111a-e063-dadaa90a10e2BELLI MOISTURIZING HAND SANITIZER - BKC 0.1% (4228-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42281-101-11BELLI MOISTURIZING HAND SANITIZER0.1 PERCENT59 mL in 1 TUBELOTION598

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42281-101BELLI MOISTURIZING HAND SANITIZER 0.1 PERCENT (BENZALKONIUM CHLORIDE) LOTION [ABT BELLI-MATERNA INC]8Legacy NDC, 1 package rows20220107_e0eb60f9-dfa3-4244-9e36-d985b8d0a187.zip

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
42281-10142281-101-11

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
ALCOHOL3K9958V90MIACT
POLYSORBATE 207T1F30V5YHIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
LEMON OILI9GRO824LLIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
d4f13c39-d5a7-5c55-e053-2a95a90aaac4e0eb60f9-dfa3-4244-9e36-d985b8d0a1872022-01-06WarningsExact identifier
spl id: d4f13c39-d5a7-5c55-e053-2a95a90aaac4
spl set id: e0eb60f9-dfa3-4244-9e36-d985b8d0a187

Reported adverse events (FAERS/openFDA)#

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