Hand Sanitizer

Manufacturer
Bullet Line, LLC
Effective date
2020-08-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:29

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (80%)

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Hand sanitizing to reduce bacteria on the skin. Recommended for repeated use.

WARNINGS SECTION

For external use only. Keep out of eyes. Keep out of reach of children. Flammable - keep away from open flame. Do not use in or near the eyes. Stop use and ask a doctor if irritation or rash appears and if swallowed contact a doctor or poison control center right away.

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Purified Water USP

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4031740317

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
19392-150-012022-01-28C16284748780-1d6a99b39-7a0a-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
19392-150-01Hand Sanitizer8 mL in 1 BOTTLE, PLASTICLIQUID81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
19392-150HAND SANITIZER (ALCOHOL) LIQUID [BULLET LINE, LLC]1Legacy NDC, 1 package rows20200822_ad640227-65ac-e213-e053-2995a90a15e2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
19392-15019392-150-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ad640db6-d507-0b51-e053-2a95a90a050bad640227-65ac-e213-e053-2995a90a15e22020-08-21WarningsExact identifier
spl id: ad640db6-d507-0b51-e053-2a95a90a050b
spl set id: ad640227-65ac-e213-e053-2995a90a15e2

Reported adverse events (FAERS/openFDA)#

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