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

Key Label Information#

Active Ingredients And Purpose

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride

OTC - PURPOSE SECTION

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

Uses

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

WARNINGS SECTION

Stop use and ask a doctor if irritation or rash occurs. Keep out of reach of children.

Directions And Dosage

DOSAGE & ADMINISTRATION SECTION

for external use only

Other Label Information

INACTIVE INGREDIENT SECTION

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

Label Images#

label
label

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#

NDC Codes#

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

Ingredients#

Complete SPL Sections#

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Sodium Chloride

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Stop use and ask a doctor if irritation or rash occurs. Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION

for external use only

Source Document#

Source XML