Bye Zero

Manufacturer
Korea Life Science
Effective date
2023-10-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:56:47

Label at a glance#

ProductBye Zero
Active ingredientMAGNESIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride

INACTIVE INGREDIENT SECTION

Kelp extract, Seaweed extract, magnesium extract, calcium extract, potassium extract, sulfate ion extract, water

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

place enough product on hadns to cover all surfaces. rub hands together until dry.

supervise children uner 6 years of age when using this product to avoid swallowing. 

WARNINGS SECTION

Stop use and ask a doctor if irritation or rash occurs.

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80762-0020-12024-07-30C16284748780-11030e365-0757-111a-e063-dadaa90a10e2fe88e417-e671-da11-e053-6294a90ac0d2
80762-0020-12024-01-30C16284748780-11030e365-0757-111a-e063-dadaa90a10e2fe88e417-e671-da11-e053-6294a90ac0d2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80762-0020-1Bye Zero90 mL in 1 BOTTLE, SPRAYLIQUID902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80762-0020BYE ZERO (MAGNESIUM) LIQUID [KOREA LIFE SCIENCE]21 package rows20231014_fe88e417-e671-da11-e053-6294a90ac0d2.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80762-002080762-0020-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
07a420ef-6915-821b-e063-6294a90a4c3efe88e417-e671-da11-e053-6294a90ac0d22023-10-13WarningsExact identifier
spl id: 07a420ef-6915-821b-e063-6294a90a4c3e
spl set id: fe88e417-e671-da11-e053-6294a90ac0d2

Reported adverse events (FAERS/openFDA)#

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