Alcohol

Manufacturer
Hello Bello | Unconditional Love
Effective date
2021-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:00

Label at a glance#

ProductAlcohol
Active ingredientAlcohol
Label structure9 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v.

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE(S):

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS:

WARNINGS SECTION

For external use only

  • Flammable
  • Keep away from heat or flame

OTC - DO NOT USE SECTION

  • Do not use: in children less than 2 months of age, on open skin wounds

OTC - WHEN USING SECTION

  • When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

  • Stop use and ask doctor if irritation or rash occurs. These may be signs of a serious condition.

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 right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

  • Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Store between 15-30C (59-86F)

  • Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Principal Display Panel – 59 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Non-sterile Solution

hello
bello™

Alcohol Antiseptic 80
Topical Solution

Hand Sanitizer
Spray

2 fl. oz. (59 ml) e

Principal Display Panel – 59 mL Bottle Label
Principal Display Panel – 59 mL Bottle Label

Principal Display Panel – 59 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

hello
bello™

Apple Blossom

62.5% Alcohol

Hand Sanitizer
Spray

2.0 fl. oz. (59 ml) e

Principal Display Panel – 59 mL Bottle Label
Principal Display Panel – 59 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286985ethanol 62.5 % Topical SprayPSN1
1241663ethanol 80 % Topical SprayPSN1
2286985ethanol 0.625 ML/ML Topical SpraySCD1
1241663ethanol 0.8 ML/ML Topical SpraySCD1
2286985ethanol 62.5 % Topical SpraySY1
1241663ethanol 80 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73418-042-01Alcohol118 mL in 1 BOTTLESPRAY1181
73418-043-01Alcohol59 mL in 1 BOTTLESPRAY591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73418-042ALCOHOL SPRAY [HELLO BELLO]1Legacy NDC, 1 package rows20210317_81bdd5e0-dd41-4fec-ae25-e0129b4048ee.zip
73418-043ALCOHOL SPRAY [HELLO BELLO]1Legacy NDC, 1 package rows20210317_81bdd5e0-dd41-4fec-ae25-e0129b4048ee.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
73418-04273418-042-01
73418-04373418-043-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
38401533-93d4-499f-872f-fb560f24d29281bdd5e0-dd41-4fec-ae25-e0129b4048ee2021-02-09WarningsExact identifier
spl id: 38401533-93d4-499f-872f-fb560f24d292
spl set id: 81bdd5e0-dd41-4fec-ae25-e0129b4048ee

Reported adverse events (FAERS/openFDA)#

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