FDA.reportPublic FDA data

Aloe Scent - A/B Hand Sanitizing Spray

Manufacturer
Custom HBC Corporation | Pluma Nacional, S.A. de C.V. | Bell Pharmaceuticals, Inc.
Effective date
2010-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:55

Label at a glance#

ProductAloe Scent A B Hand Sanitizing
Active ingredientALCOHOL
Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Ethyl Alcohol (62 percent)

INACTIVE INGREDIENT SECTION

Also contains: Purified Water, Propylene Glycol, Glycerin, Aloe Vera, Vitamin E Acetate, Fragrance.

WARNINGS SECTION

Warning:

Flammable. Keep away from open flame

DESCRIPTION SECTION

8ml / 0.25 ozs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aloe Scent - A/B Hand Sanitizing Spray

(10601-0.25)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SprayLabelSprayLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020364ethanol 62 % Topical SprayPSN1
1020364ethanol 0.62 ML/ML Topical SpraySCD1
1020364ethanol 62 % Topical SpraySY1
1020364ethyl alcohol 62 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42825-100-082020-01-31C16284748780-19d75b9d0-8a0d-f424-e053-dadaa90a57ceAloe Scent - A/B Hand Sanitizing Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42825-100-08Aloe Scent A B Hand Sanitizing8 mL in 1 BOTTLE, SPRAYSPRAY81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42825-100ALOE SCENT A B HAND SANITIZING (ALCOHOL) SPRAY [CUSTOM HBC CORPORATION]1Legacy NDC, 1 package rows20100626_c1e585df-7e5a-4363-aac0-3958c39cb6da.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42825-10042825-100-08

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB

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
e6f3adb8-c116-4124-acdd-3f2283edc79dc1e585df-7e5a-4363-aac0-3958c39cb6da2010-06-25WarningsExact identifier
spl id: e6f3adb8-c116-4124-acdd-3f2283edc79d
spl set id: c1e585df-7e5a-4363-aac0-3958c39cb6da

Reported adverse events (FAERS/openFDA)#

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